Food Recalls

Tulkoff Food Products, Inc. Issues Allergy Alert on Undeclared (Soy and Wheat) in Kimchi Aioli

June 8, 2021

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Tulkoff Food Products Inc. of Baltimore Maryland is recalling Kimchi Aioli 18 fl. oz. squeeze bottles with lot code 09.18.2021M for the presence of undeclared wheat and soy allergens.
People who have an allergy or severe sensitivity to wheat or soy run the risk of serious or life-threatening allergic reaction if they consume these products.
Tulkoff Kimchi Aioli was distributed on the East coast through US Foods, Pastores, and Restaurant Depot during the dates of March 22, 2021, and June 6th, 2021. Affected states are Connecticut, Delaware, Massachusetts, Maryland, New Jersey, New York, Pennsylvania, Rhode Island, and Virgina.
No illnesses or adverse reactions have been reported as of 6/8/2021.
The affected product is in a clear plastic squeeze 18 fl. oz. bottle. The front label will say Kimchi Aioli, while the back label will say Jalapeno Aioli. The Best if used by Date 09.18.2021M will be printed on the back of the bottle.
The recall was initiated after Tulkoff discovered that the incorrect back label had been affixed to the product. This error was confined to one specific product, and one specific lot. One hundred and forty (140) cases of the product were made. No other products manufactured by Tulkoff Food Products, Inc. are at risk.
Customers who have purchased Tulkoff Kimchi Aioli 18 fl oz lot 09.18.2021M are urged to destroy the product and or return it to the place of purchase for a full refund. Consumers with questions may contact Tulkoff Food Products Inc, customer service at 1-800-638-7343, Monday through Friday, between the hours of 8:00am (EST) and 5:00pm (EST).
The Kimchi Aioli can be identified as follows:
Package Size    Package Label    Product Detail    Lot # on Pkg.
18 fl. oz. Clear plastic squeeze bottle    Tulkoff    Kimchi Aioli 18 oz    Best if Used By
09.18.2021M

Smilin’ Bob’s Voluntarily Recalls Smilin’ Bob’s Smoked Fish Dip Products Because of Possible Health Risk

June 8, 2021

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Smilin’ Bob’s is voluntarily recalling Smilin’ Bob’s Original Smoked Fish Dip and Smilin’ Bob’s All Natural Smoked Fish Dip. This recall is being initiated as a result of the Banner Smoked Fish, Inc. recall of smoked fish due to possible contamination with Listeria monocytogenes. Smilin’ Bob’s used the recalled smoked fish from Banner Smoked Fish, Inc in the products listed below. The recall is issued only for products listed below.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
No illnesses have been reported to date.
Smilin’ Bob’s is working with distributors and retailers to quarantine and recover any impacted product remaining on store shelves. A total of 1,261 cases were distributed to retailers in the states of FL, GA, AL, SC, TN, NC, and VA.
HOW TO IDENTIFY THE RECALLED PRODUCT:
The containers have the “Best If Use By” dates stated below printed on the side of each container and the lot number stated for each product on the side or the lid (see attached pictures). This recall applies only to the products with the “Best If Use By” dates stated below.
Product    Size    Best If Used By dates
Printed on container side    12 Pack
Case    Date of
Distribution
Smilin' Bob's Key West
Style Original Smoked
Fish Dip    8 ounce round
plastic container    Aug 03 2021
Aug 10 2021    878 cases    May 24 2021
June 4 2021
Smilin' Bob's Key West
Style Original Smoked
Fish Dip    15.5 ounce
plastic container    Aug 03 2021
Aug 10 2021    335 cases    May 27 2021
May 25 2021
May 31 2021
Smilin' Bob's All Natural
Smoked Fish Dip    8 ounce round
plastic container    Aug 10 2021    48 cases    June 4 2021
Smilin’ Bob’s determined to voluntarily recall the products listed after being notified that Banner Smoked Fish. Inc. had expanded its recall.
Product safety and consumer confidence is of utmost importance to Smilin’ Bob’s and its customers. Consumers who have purchased any of the recalled products listed above are urged to immediately return them to the place of purchase for a full refund. Consumers with questions may call 305-395-8382 at any time.
This recall is being done with the knowledge of the Food and Drug Administration.

Olde Thompson LLC Issues A Voluntary Recall of Olde Thompson And Sun Harvest Organic Ground Coriander Due to Possible Salmonella Risk

June 4, 2021

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Olde Thompson LLC. Oxnard, CA in cooperation with the FDA is recalling Olde Thompson and Sun Harvest Organic Ground Coriander in 1.5oz glass jar with flip top closure, Lot # 23632 and 23631 due to possible contamination by Salmonella.
To date no illness have been reported. If you have the recalled product, please do not consume it. Please dispose of the recalled product and its container.
Salmonella is known to cause salmonellosis in humans and animals. Symptoms of salmonellosis include diarrhea, abdominal cramps and fever and are known in some cases to be severe enough to require hospitalization and can cause serious complications or death in young children, the elderly, or a person with a compromised immune system. If you have already consumed the product and have concerns about your health, please consult your healthcare provider.
Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers immediately.
The recalled product is identified and distributed as follows:
Olde Thompson Organic Ground Coriander 1.5oz. in glass jar with flip-top lid.
Sun Harvest Organic Coriander 1.5oz in glass jar with flip-top lid.
UPC code: 400000290942
Sold at Homegoods, Jungle Jim’s International Market and Smart and Final in AZ, CA, Ga, NJ, IN,
and OH between May 26th and June 4th, 2021.
The recall affects 626 units Olde Thompson Organic Ground Coriander 1.5oz in glass jar and 150 units of
Sun Harvest Organic Ground Coriander 1.5oz in glass jar.
Lot # (s): 23632, 23631 located on the bottom of the jar.
No illnesses have been reported.
The bacterium was discovered during routine sampling of raw materials.
Customers who have purchased these products and have any questions should contact
a Olde Thompson Customer Care representative at 1-805-793-4888
Available: Monday – Friday, 7:30AM – 5PM PST. Saturday, 9AM – 5PM PST. and Sunday,
NOON – 5PM PST.

Banner Smoked Fish Recalls Smoked Fish Products, Salads, Pickled Fish Products, and Cream Sauce Products Because of Possible Health Risk

June 4, 2021

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Banner Smoked Fish, Inc. of Brooklyn, NY is voluntarily expending recalling its SMOKED FISH, SALADS, PICKLED FISH PRODUCTS, and CREAM SAUCE PRODUCTS (product names and photos of labels are listed below) of all products within expiry, in all package sizes, all package types and all lots. The recall is because the products have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled smoked fish were distributed through retails and distributions, also online purchasing in NY, NJ, IL, PA, CA, FL, NE, AZ, MA, MD, VA, NV, OR, WI, NC, SC, and GA area.
The product comes in various sizes in both air pack and vacuum packages. The lot number or sell by date are placed on the back of the package.
The products were found to be processed under unsanitary condition. The problem was discovered through FDA routine inspection. No illnesses have been reported to date in connection with this problem.
Consumers who have purchased these items are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at (718) 449 – 1400 Monday to Friday from 8 AM – 4 PM EST.
     Product name
1.            Barbeque Spiced Smoked Nova Salmon
2.            Brook Trout
3.            Center Sliced Smoked Norwegian Style Salmon
4.            Everything Spiced Smoked Nova Salmon
5.            Finest Sliced Salty Lox
6.            Finest Sliced Smoked Nova Salmon
7.            Irish Cured Smoked Salmon
8.            Lox Trimmings
9.            Mackerel
10.          Naturally Smoked Nova Salmon
11.          Noon Hour Smoked Salmon
12.          Norwegian Style Smoked Salmon
13.          Nova Atlantic Salmon
14.          Nova Bits
15.          Nova Homarus
16.          Nova Lox
17.          Nova Salmon
18.          Nova Salmon Bagel Cuts
19.          Pastrami Nova Atlantic Salmon
20.          Pastrami Style Smoked Nova Salmon
21.          Pepper Crusted Smoked Nova Salmon
22.          Presliced Gravad Lox
23.          Presliced Pastrami Style Salmon
24.          Presliced Pastrami Style Salmon
25.          Presliced Scotch Style Salmon
26.          Presliced Scotch Style Salmon
27.          Presliced Scotch Style Smoked Salmon
28.          Presliced Smoked Atlantic Salmon
29.          Sable
30.          Sliced Gravlax
31.          Sliced Pastrami Style Nova
32.          Sliced Smoked Norwegian Style Salmon
33.          Sliced Smoked Salmon
34.          Sliced Smoked Scotch Style Salmon
35.          Smoked Nova Bagel Cuts
36.          Smoked Nova Lox
37.          Smoked Nova Salmon
38.          Smoked Sliced Nova Salmon
39.          Smoked Trout
40.          Somga
41.          Trimmed Nova
42.          Whitefish
43.          5 LB HERRING SALAD
44.          5 LB WHITEFISH SALAD
45.          5 LB KIPPERED SALMON SALAD
46.          ATLANTIC NOVA SALMON
47.          BROOK TROUT FILLET
48.          CHILE LOX
49.          CHUNKS
50.          COLD SMOKED TUNA
51.          COLD SMOKED WHITEFISH
52.          CREAM SAUCE
53.          DRY WHITEFISH
54.          EUROPEAN GOURMET NOVA SALMON
55.          GRAVAD LOX
56.          GROUND NOVA
57.          HOMARUS NORWEGIAN
58.          KIPPERED SALMON
59.          KIPPERED SALMON MEAT
60.          MARSHALL NOVA
61.          PEPPER CRUSTED SMOKED NOVA
62.          PICKLED HERRING FILLET
63.          PICKLED LOX
64.          PRESLICED SMOKED NOVA SALMON
65.          SCOTCH STYLE SALMON
66.          SEABASS
67.          SLICED ESCOLAR
68.          SLICED SABLE
69.          SLICED SMOKED NOVA SALMON
70.          SLICED SMOKED NOVA TRAY
71.          SLICED SMOKED PASTRAMI STYLE NOVA
72.          SMOKED ESCOLAR
73.          SMOKED CHUBS
74.          SMOKED PASTRAMI STYLE SALMON
75.          HERRING TID BITS IN CREAM
76.          HERRING TID BITS IN WINE
77.          TROUT
78.          TURBOT
79.          WHITEFISH MEAT
80.          WHITEFISH SALAD MARSHALL
81.          HERRING WHOLE FILLETS IN WINE
82.          WHOLE LOX

Sun Hong Foods, Inc. Recalls Seafood Mushroom Because of Possible Health Risk

June 1, 2021

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Sun Hong, Inc 1105 W Olympic Blvd, Montebello, CA 90640 is recalling All Cases of Seafood Mushroom (Product of China) Net Wt 5.3 oz./150g because it has the potential to be contaminated with Listeria monocytogenes, a bacterium which can cause life-threatening illness or death. Consumers are warned not to consume even if it does not look or smell spoiled.
Listeria monocytogenes, an organism which can cause serious , and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria monocytogenes can cause miscarriages and stillbirths among pregnant women.
Product was distributed (CA, TX, WA, IL, FL)
Stores that may carry our brand: Asian Supermarkets
Seafood mushrooms are packaged inside has 40 packs of 150g single packages
Seafood mushrooms are white mushrooms, with long, long white stems, and mushroom caps. They are usually sold in clusters. The affected products are sold in a clear plastic tray that is packed in green and clear plastic. “100% Natural fresh” is printed in the top right. “Mushrooms” is written in cursive and in light green in the middle. The top half is clear and the bottom is dark green with a white stripe going across. “Seafood Mushroom” is printed in light green and white on the bottom half. Beneath that are instructions to keep it refrigerated and its weight of 5.3oz/150g.
•    UPC 6 953150 011881
•    Brand name on the back: Sun Hong Foods, Inc
•    Packaging 5.3oz/ 150g
•    Sold under refrigerated conditions
Sun Hong Foods became aware of this issue after notification by the CDPH that samples of the product tested by the State of California were found to be positive for Listeria monocytogenes
Status of the number and types of illnesses that have been confirmed to date – or that there are no illnesses reported to date
Consumers who have purchased Sun Hong Foods, Inc Seafood Mushrooms are urged to not eat it and return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1 (323) 597-1112, Monday-Friday 8:00 AM - 4:00 PM PST. Thank you.

Concord Farms Recalls Enoki Mushrooms Due to Possible Health Risk

May 29, 2021

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CONCORD FARMS of Vernon, CA is recalling enoki mushrooms grown in Korea, because it has the potential to be contaminated with listeria monocytogenes, a bacterium which can cause life-threatening illness.
Symptoms of listeria may include fever, muscle aches, severe headache, nausea, vomiting, stiff neck, confusion, loss of balance, and convulsions. People experiencing these problems should seek immediate medical attention. This bacteria can be completely destroyed and the risk of infection can be eliminated by thoroughly cooking foods at temperatures of 165°F (73.8°C).
Mushrooms are fungi, meaning they are not vegetables or fruits. Consumers should never eat mushrooms raw. All surfaces, utensils or containers that are used for preparing mushrooms should be separated from other foods to avoid cross-contamination.
Product was distributed from California to retail stores through produce distributors. Product is packaged in a black, yellow and transparent plastic packaging, with the “Concord Farms” logo above “fresh enoki mushrooms”. Enoki mushrooms are white, stringy with small caps. The weight of the products are 5.3 oz (150g) or 7 oz (200g). The UPC barcode numbers are 049995041049.
No infections have been reported or confirmed. Consumers who have purchased our enoki mushrooms are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 323-582-6000 Monday to Friday, 7am to 3pm PST.

Marquis Worldwide Specialty Inc. Recalls Organic Enoki Mushroom 200g Because of Possible Health Risk

May 29, 2021

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Marquis Worldwide Specialty Inc of City of Industry, CA is recalling All of the Organic Enoki Mushroom 200g, because it has the potential to be contaminated with Listeria monocytogenes, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Listeria monocytogenes can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. People experiencing these problems should seek immediate medical attention.
Organic Enoki mushroom 200g was distributed nationwide from California and it reached to consumers through retail stores and other produce wholesalers.
It is packed by each 200g individual plastic package and the package is clear on top and orange on the bottom part. It has ‘Conah Organic enoki mushroom’ written on front.
The mushroom is white and has almost no smell. As it is vegetable, it does not have a clear date of expiration.
No illnesses have been reported to date in connection with this problem.
We are investigating to determine where contamination occurred. Consumers who have purchased 200g packages of ‘Conah Organic Enoki Mushroom’ are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-626-810-6426 Monday – Friday 7 am to 4 pm.

Rainfield Marketing Group, Inc. of Vernon, CA is Recalling Enoki Mushrooms (Product of Korea) Because it has the Potential to be Contaminated with Listeria monocytogenes

May 29, 2021

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Rainfield Marketing Group, Inc. of Vernon, CA is recalling all cases of its 150g packages of Enoki Mushrooms (Product of Korea) because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled products were distributed to CA, MD, and TX through produce distributors or wholesalers to retail stores nationwide.
The Enoki comes in a 150g, clear plastic and orange packaging with the description “Enoki Mushroom” in English and labeled “Product of Korea” along with “Must be cooked enough for a minimum of 3-10 minutes at 70°C, DO NOT CONSUME RAW”. On the back left of packaging, there is UPC code 085412004020 and below Distributed by Rainfield Marketing Group, on the right a list of Nutrition Facts.
No illnesses have been reported to date.
The potential for contamination was noted after routine testing by California Department of Public health revealed the presence of Listeria monocytogenes in 150g package of Enoki.
The distribution of the product has been suspended.
Consumers who have purchased 150g packages of Enoki are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at (323) 825-2825. Monday-Friday 7:00AM to 4:00PM.

California Terra Garden Inc. Recalls Seafood Mushroom Because of Possible Health Risk

May 29, 2021

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California Terra Garden Inc. of Commerce, CA is recalling all cases of its 150g/5.3-ounce packages of Seafood Mushroom (Product of China) because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled products were distributed from California through produce distributors or wholesalers to retail stores nationwide.
The Seafood mushroom comes in a clear plastic package with the description “Seafood Mushroom” in English and French, and Guan’s logo in the front. At the back, there is UPC code, 859267007501. Product code is 3460 at the back top right.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after routine testing by California Health Department revealed the presence of Listeria monocytogenes in one 150g package of Seafood mushroom.
The distribution of the product has been suspended.
Consumers who have purchased any package of Seafood mushroom are urged to return them to the place of purchase for a full refund. Consumers with question may contact the company at 323.597.0346, Monday to Friday 9 am to 4 pm.

The Kroger Co. is Voluntarily Recalling its Chicken Street Taco Kit Due to Undeclared Egg

May 28, 2021

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The Kroger Co. is voluntarily recalling its Chicken Street Taco Kit due to a recall issued by its supplier Reser’s Fine Foods. These bulk kits have Chipotle Crema Sauce, which contains egg that was not declared on the label. Consumers who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume these products.
The voluntary recall includes the Chicken Street Taco Kits, which were sold in deli cases in black plastic trays with clear plastic lids (see picture below) with the UPC 41573-71252 and only product purchased before May 25, 2021.
All affected products were pulled from our deli cases on May 22, 2021 and relaunched on May 27, 2021 with the correct labels.
The products were distributed by Kroger grocery stores under a variety of banner names in these states: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Delaware, Florida, Georgia, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maryland, Michigan, Mississippi, Missouri, Montana, Nebraska, Nevada, New Mexico, North Carolina, Ohio, Oregon, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin and Wyoming.
To date, there have been no reports of illness or complaints involving the product addressed in this recall.
Customers with an egg allergy or sensitivity who have purchased the affected product are urged not to consume it and dispose of it or return it to their local store for a full refund.
Customers who have questions may contact Kroger at 1-800-KROGERS Monday through Friday, 8:00 AM to 12:00 AM EST, and Saturday and Sunday, 8:00 AM to 9:30 PM EST.

King's Command Foods, LLC. Recalls Meat and Poultry Meatballs and Pork Pattie Products Due to Misbranding and Undeclared Allergens

May 28, 2021

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King's Command Foods, LLC., a Kent, Wash. establishment, is recalling approximately 20,025 pounds of fully cooked, not shelf stable meat and poultry meatballs and pork patties due to misbranding and undeclared allergens, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today. The product contains egg, milk, and/or wheat, known allergens, which is not declared on the product label. 
The fully cooked, not shelf stable meat and poultry items were produced January 08, 2021, January 15, 2021, and March 03, 2021. The following products are subject to recall:
•    10-lb. bulk-packed cases containing "3.75 oz RIB SHAPED PORK PATTIES WITH BBQ SAUCE" with code 2549616/72314 and "USE BY 3/2/2022," that contain undeclared wheat which is not represented on the label.
•    15-lb. bulk-packed cases containing "3.0 oz RIB SHAPED PORK PATTIES WITH BBQ SAUCE" with code 72314 and "USE BY 3/2/2022", that contain undeclared wheat which is not represented on the label.
•    15-lb. bulk-packed cases containing "0.50oz SWEDISH MEATBALLS" with code 72148 and "USE BY 1/7/2022", containing undeclared egg which is not represented on the label.
•    14-lb. bulk-packed cases containing "0.50oz SWEDISH MEATBALLS WITH SAUCE" with code 72147 and "USE BY 1/7/2022", containing undeclared egg which is not represented on the label.
•    10-lb. bulk-packed cases containing "0.5 OZ CHICKEN AND BEEF MEATBALLS" with code 72180 and "USE BY 1/7/2022", containing undeclared milk which is not represented on the label.
•    10-lb. bulk-packed cases containing "0.50 oz MEATBALLS" with code 01380 displayed beneath the barcode and "USE BY 1/14/2022," containing undeclared egg and milk which is not represented on the label.
•    10-lb. bulk-packed cases containing ".5 oz HOMESTYLE MEATBALLS" with code 00133 and "USE BY 1/7/2022," containing undeclared milk which is not represented on the label.
•    20-lb. bulk-packed cases containing ".5 OZ ITALIAN STYLE MEATBALLS" with code 72182 and "USE BY 3/2/2022," containing undeclared egg which is not represented on the label.
The products subject to recall bear establishment number "EST. M1515A" inside the USDA mark of inspection. These items were distributed for food service use in California, Idaho, Illinois, Minnesota, Missouri, North Carolina, Oregon, Texas, Virginia, and Washington.
The problem was discovered when the establishment determined that allergen-containing ingredients may have comingled with the recalled products that do not normally contain the identified allergens.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
FSIS is concerned that some product may be in food service freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
Consumers and members of the media with questions about the recall can contact King's Command Foods, LLC Customer and Consumer Hotline at (800)-829-2838.

Hy-Vee Issues Allergy Alert on Undeclared Egg in Chicken Street Taco Kit Due to Reser’s Fine Foods Recall

May 27, 2021

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Hy-Vee, Inc., based in West Des Moines, Iowa, is voluntarily recalling its Chicken Street Taco Kit due to a recall issued by its supplier Reser’s Fine Foods. Hy-Vee received bulk Chicken Taco Kits from Reser’s Fine Foods and repackaged them into Hy-Vee Chicken Street Taco kits. These bulk kits contained Chipotle Crema Sauce which contains egg that was not declared on the label. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume these products.
The voluntary recall includes the Hy-Vee Chicken Street Taco Kits which were sold in deli cases in black plastic trays with clear plastic lids (see picture below) with the UPC 02-82503-09993 and a “Best If Use By” date prior to May 27, 2021 (located on top of label).
The products were distributed by Hy-Vee grocery stores across its eight-state region of Iowa, Illinois, Missouri, Kansas, Nebraska, South Dakota, Minnesota and Wisconsin.
To date, there have been no reports of illness or complaints involving the product addressed in this recall.
Customers with an egg allergy or sensitivity who have purchased the affected product are urged not to consume the product and dispose of it, or return it to their local Hy-Vee store for a full refund.
Consumers with questions may contact Hy-Vee Customer Care representatives 24 hours a day, seven days a week at 1-800-772-4098.

Giant Eagle Voluntarily Recalls Chicken Street Taco Kit

May 26, 2021

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Giant Eagle, Inc. has issued a voluntarily recall of Chicken Street Taco Kits due to the possibility the product may contain an undeclared egg allergen. Those who have an allergy or severe sensitivity to eggs could experience a serious or life-threatening allergic reaction if they consume these products.
The impacted products have “sell by” dates through 05/28/21 and can be identified by PLU 56598 located in the upper right corner of the item’s scale tag. The recalled items were sold in the prepared foods departments at Giant Eagle and Market District locations in PA, OH, MD, and IN.
Giant Eagle was made aware of the issue by its supplier partner, Reser’s Fine Foods, when they discovered the product was missing the egg allergen declaration in one of the ingredients, chipotle crema. There has been no reported illness associated with this recall.
Customers who have purchased the affected product should dispose of it and return a qualifying receipt to their local Giant Eagle or Market District store for a refund. Customers with questions may call Giant Eagle Customer Care at 1-800-553-2324 Monday through Friday 9 a.m. to 9 p.m. EST.
In addition to this public communication regarding this recall, Giant Eagle initiated its consumer recall telephone notification process. The consumer recall process uses purchase data and consumer telephone numbers housed in the Giant Eagle Advantage Card database to alert those households that purchased the affected product and have updated telephone contact information in the database.

Gilster-Mary Lee Corp. Issues a Recall for Undeclared Milk Allergen in Full Circle Organic Microwave Popcorn Salted

May 26, 2021

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Gilster-Mary Lee, 8366 North Highway 51, McBride, Missouri, is voluntarily recalling one lot of Full Circle Organic Microwave Popcorn Salted, UPC 36800-40611 at the consumer level because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.
The only lot involved is Full Circle Organic Microwave Popcorn Salted, packaged in 9.9-oz. cartons which have a Best By date of APR 09 22 N2 (UPC# 36800-40611). Consumers should return the product to the store for a full refund or discard it.
The product was distributed to TOPCO Members Distribution Centers in Schenectady, NY; Chandler, AZ; Lathrop, CA; Farr West, UT; Pembroke, NH; Milton, PA; Byron Center, MI; Cheshire, CT and St. Cloud, MN. Gilster-Mary Lee Corp. became aware of the mispackaging after receiving an email from a customer warehouse. No illnesses have been reported to date in connection with this popcorn.
For questions, consumers can call Gilster-Mary Lee Corp. at 618-826-2361 ext. 3283, from 8:00 am to 4:30 pm CST Monday - Friday.

Legacy Food Company, Inc. Recalls Beef Jerky Products Due to Misbranding and an Undeclared Ingredient

May 26, 2021

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– Legacy Food Company, Inc., a Rancho Cucamonga, Calif. establishment, is recalling approximately 67,895 pounds of beef jerky due to misbranding and an undeclared ingredient, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains sesame oil, which is not declared on the product label. 
The beef jerky items were produced on various dates from July 20, 2020 through May 14, 2021. The following products are subject to recall: [View Labels (PDF Only)]
•    10-lb. packages containing “N4 Vua Kho Bo Curry Beef Jerky.”
•    10-lb. packages containing “N8 Vua Kho Bo Flank Steak Beef Jerky Fish Sauce.”
•    10-lb. packages containing “N9 Vua Kho Bo House Special Beef Jerky Fish Sauce.”
•    10-lb. packages containing “Vua Kho Bo Hot Beef Jerky.”
•    10-lb. packages containing “Hot Peppered Beef Jerky.”
•    16-oz packages containing “Formosa Brand Hot Peppered Beef Jerky.”
The 10-lb products subject to recall bear establishment number “Est. 8256” and the 16-oz product listed above bears establishment number “EST 2446” inside the USDA mark of inspection. These items were sold online and shipped to retail stores in California. The 10-lb products are sold in bulk packaging and were removed from their original packaging and repackaged and relabeled for online sales. Retail stores remove the products from their original packaging and display them in bins for sale.
The problem was discovered during routine FSIS label verification activities when it was determined that the labels did not accurately list all sub-ingredients.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
Members of the media with questions about the recall can contact Tony Kan, President/CEO, Legacy Food Company, at (909) 244-0865. Consumers with questions about the recall can contact Kevin Yang, Office Manager, Legacy Food Company, at (909) 244-0865.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Medically Minded Hand Sanitizer– Nationwide Recall Expansion Due to The Presence of Undeclared Methanol

May 25, 2021

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Medically Minded Hand Sanitizers:
8 oz. UPC 676753004208; Lot E332020, Lot E212020, and Lot E082020
8.5 oz. UPC 676753004147; Lot E372020
10 oz. UPC 676753004178 Lot GV4420205
All above lots have Best By Date of 5/21/2022.
This recall has been initiated due to the presence of undeclared Methanol. Use of or consumption of this product can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma & or permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. Methanol was discovered through lab testing.
To date, Global Sanitizers has not received any reports of adverse events related to this recall.
We began shipping this product on approximately July 10, 2020.
Immediately examine your inventory and quarantine product subject to recall. In addition, if you may have further distributed this product, please identify your customers and notify them at once of this product recall. Your notification to your customers may be enhanced by including a copy of this recall notification letter. If you have these recalled items in stock, please send an email to recall@globalsanitizers.com and we provide further instructions for product destruction.
This recall should be carried out at the consumer level.
Your assistance is appreciated and necessary to prevent consumer illness or patient harm.
Please email recall@globalsanitizers.com for further instructions.
If you have any questions, call Ryan at 702.323.4402
This recall is being made with the knowledge of the Food and Drug Administration.

Milan Provisions Co. Inc. Recalls Jalapeno Chorizo Sausage Products Formulated With Pork Ingredients Produced Without the Benefit of Inspection

May 21, 2021

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Milan Provisions Co. Inc., a Corona, N.Y. establishment, is recalling approximately 6,000 pounds of heat-treated, not fully cooked, not shelf stable chorizo sausage products made using a pork ingredient produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The jalapeno chorizo sausage items were produced from April 13, 2021 through April 16, 2021. The following product is subject to recall: [View Labels (PDF Only)]
•    14-oz and 22-oz vacuum-packed packages containing “MILAN PROVISIONS MEXICAN BRAND MADE IN NEW YORK CURED CHORIZO JALAPEÑO” with expiration dates of “JUN 12 21”, “JUN 13 21”, “JUN 14 21” and “JUN 15 21.”
The products subject to recall bear establishment number “EST. 4335” inside the USDA mark of inspection. These items were shipped to retail locations in New York.
The problem was discovered when FSIS determined that the firm received pork trim product from a retail butcher facility that is not federally inspected and used it in production of the chorizo product.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.  
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Salvatore Laurita, President, Milan Provisions Co. Inc., at (718) 899-7678.

Randall Foods Inc. Initiates Voluntary Recall of all Randall Beans

May 20, 2021

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Randall Foods, Inc. of Cincinnati, Ohio is recalling all its Randall-brand beans because of manufacturing deviations that may pose a potential health risk.  The recall includes the following products:
Brand    Description    UPC    Batch/Lot Numbers    “Best By” Date
Randall    RANDALL GREAT NORTHERN BEANS 48OZ    070095000100    ALL    Prior to January 1 2025
Randall    RANDALL GREAT NORTHERN BEANS 24OZ    070095000117    ALL    Prior to January 1 2025
Randall
Randall    RANDALL GREAT NORTHERN BEANS 15.4OZ
RANDALL PINTO BEANS 48OZ    070095000131
070095000209    ALL
ALL    Prior to January 1 2025
Prior to January 1 2025
Randall    RANDALL PINTO BEANS 24OZ    070095000216    ALL    Prior to January 1 2025
Randall    RANDALL PINTO BEANS 15.4OZ    070095000230    ALL    Prior to January 1 2025
Randall    RANDALL MIXED BEANS 48OZ    070095000407    ALL    Prior to January 1 2025
Randall    RANDALL MIXED BEANS 24OZ    070095000414    ALL    Prior to January 1 2025
Randall    RANDALL MIXED BEANS 15.4OZ    070095000430    ALL    Prior to January 1 2025
Randall    RANDALL KIDNEY BEANS 48OZ    070095000308    ALL    Prior to January 1 2025
Randall    RANDALL KIDNEY BEANS 24OZ    070095000315    ALL    Prior to January 1 2025
Randall    RANDALL KIDNEY BEANS 15.4OZ    070095000339    ALL    Prior to January 1 2025
Randall    RANDALL NAVY BEANS 48OZ    070095000506    ALL    Prior to January 1 2025
Randall    RANDALL NAVY BEANS 15.4OZ    070095000537    ALL    Prior to January 1 2025
Randall    RANDALL BLACK BEANS 48OZ    070095000605    ALL    Prior to January 1 2025
Randall    RANDALL BLACK BEANS 24OZ    070095000612    ALL    Prior to January 1 2025
Randall    RANDALL BLACK BEANS 15.4OZ    070095000636    ALL    Prior to January 1 2025
Randall    RANDALL GARBANZO BEANS 24OZ    070095000711    ALL    Prior to January 1 2025
Randall    RANDALL GARBANZO BEANS 15.4OZ    070095000735    ALL    Prior to January 1 2025
Randall    RANDALL ULITMATE 4-BEAN MIX 48OZ    070095000902    ALL    Prior to January 1 2025
Randall    RANDALL ORGANIC GREAT NORTHERN BEANS 48OZ    070095005105    ALL    Prior to January 1 2025
The product is sold in 48oz, 24oz, and 15.4oz glass jars with tan labels with “Randall” at the label top.    Approximately 1.6 million cases of affected products were distributed between March 1, 2019 and May 15, 2021 at retail locations in the following states: Alabama, Arkansas, Florida, Iowa, Illinois, Kansas, Kentucky, Michigan, Minnesota, Missouri, Nebraska, North Carolina, New York, Ohio, Oklahoma, Pennsylvania, South Dakota, Tennessee, Texas, Virginia, Wisconsin, and West Virginia.
The manufacturing deviations included a nonfunctioning temperature indicating device raising the possibility that the product was not effectively processed. Processing at temperatures below a required temperature could create a condition that could lead to premature spoilage or food borne illness; however, there have been no illnesses reported. The company is issuing this voluntary recall as a precaution.
Consumers who have purchased jars of Randall-brand beans, regardless of the “Best By” date, should return them to the place of purchase for a full refund.  Consumers with questions may contact the company between 9 am and 5 pm at 1-513-793-6525.

Interstate Food Products Recalls Little Hatches Jalapeno Cream Cheese Because of Possible Health Risk

May 20, 2021

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Interstate Food Products of Lakewood Colorado, is recalling its 14 ounce containers of Little Hatches Jalapeno Cream Cheese because they have the potential to be contaminated with Listeria monocytogenes, an organism which may cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled Little Hatches Jalapeno Cream Cheese were distributed in 6 Whole Foods stores. UPC code is 63818396147.
The product comes in a 14 ounce, clear plastic package marked with sell by date of 05/21 on top of container.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after routine testing by the FDA revealed the presence of Listeria monocytogenes in 14 ounce packages of Little Hatches Jalapeno Cream Cheese.
Product was delivered to Whole Foods stores in the Denver Colorado Metro area.
Consumers who have purchased 14 ounce containers of " Little Hatches Jalapeno Cream Cheese are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 720-626-9917, Monday thru Friday 9:00 to 3:00 EDT.

Primary Colors Design Corp Issues Allergy Alert on Undeclared Egg on Peppa Pig Chocolate Chip Cookies Gable Box

May 20, 2021

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Primary Colors Design Corp of Ashland, OH is recalling Chocolate Chip Cookies Gable Box with UPC 84512050159 because it may contain undeclared egg allergen. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume these products.
Peppa Pig Chocolate Chip Cookies were distributed to Marshalls Distribution Center in Georgia which were further distributed to Marshalls Stores. Primary Colors Design Corp did not distribute the affected recalled product of Peppa Pig Chocolate Chip Cookie Gable Boxes to any other states or retailers.
Peppa Pig Chocolate Chip Cookie Gable can be identified in a 7.0oz corrugate box with expiration date of 09/18/2021 on the top right of the handle and lot code of 091820 on the cookie bag.
No illness or customer complaints have been reported to date.
The recall was initiated after it was discovered that Peppa Pig Chocolate Chip Cookie Gables were distributed in packaging that did not reveal the presence of egg. Subsequent investigation indicates the problem was caused by inadvertently filling the box with another chocolate chip cookie, potentially exposing consumers to an undeclared allergen: egg.
Consumers who have purchased the Peppa Pig Chocolate Chip Cookie with the affected lot code are encouraged to notify Primary Colors Design Corp at sales@primarycolorscorp.com or 419- 903-0403 during normal business hours (8:00am – 5:00pm EST, Monday- Friday).

Primary Colors Design Corp Issues Allergy Alert on Undeclared Egg on Peppa Pig Chocolate Chip Cookies Gable Box

May 20, 2021

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Primary Colors Design Corp of Ashland, OH is recalling Chocolate Chip Cookies Gable Box with UPC 84512050159 because it may contain undeclared egg allergen. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume these products.
Peppa Pig Chocolate Chip Cookies were distributed to Marshalls Distribution Center in Georgia which were further distributed to Marshalls Stores. Primary Colors Design Corp did not distribute the affected recalled product of Peppa Pig Chocolate Chip Cookie Gable Boxes to any other states or retailers.
Peppa Pig Chocolate Chip Cookie Gable can be identified in a 7.0oz corrugate box with expiration date of 09/18/2021 on the top right of the handle and lot code of 091820 on the cookie bag.
No illness or customer complaints have been reported to date.
The recall was initiated after it was discovered that Peppa Pig Chocolate Chip Cookie Gables were distributed in packaging that did not reveal the presence of egg. Subsequent investigation indicates the problem was caused by inadvertently filling the box with another chocolate chip cookie, potentially exposing consumers to an undeclared allergen: egg.
Consumers who have purchased the Peppa Pig Chocolate Chip Cookie with the affected lot code are encouraged to notify Primary Colors Design Corp at sales@primarycolorscorp.com or 419- 903-0403 during normal business hours (8:00am – 5:00pm EST, Monday- Friday).

Kraft Heinz Foods Company Recalls Chef Francisco Soup Product Due to Misbranding and Undeclared Allergens

May 17, 2021

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Kraft Heinz Foods Company, a Cedar Rapids, Iowa establishment, is recalling approximately 13,504 pounds of a frozen foodservice soup product due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains milk and eggs, known allergens, which are not declared on the product label. 
The frozen soup product was produced on October 7, 2020. The following product is subject to recall: [View Labels (PDF Only)]
•    4-lb. tubs containing “Chef Francisco Minestrone Condensed Soup” with a “Chef Francisco Vegetable Beef and Barley Condensed Soup” label with lot code LD28120FT1 represented on the label. The product was distributed in 16-lb cases labeled as “Chef Francisco Minestrone Condensed Soup” with lot code LD28120FT1.
The product subject to recall bears establishment number “EST. 15818A” inside the USDA mark of inspection. This foodservice item was shipped to hotels, restaurants, and institutions nationwide.
The problem was discovered after the firm received foodservice customer complaints that the product labeled as vegetable beef and barley condensed soup contained minestrone condensed soup.
There have been no confirmed reports of adverse reactions due to consumption of this product. Anyone concerned about an injury or illness should contact a healthcare provider.  
FSIS is concerned that some product may be in the freezers of hotels, restaurants, and institutions. These businesses are urged not to serve the product. This product should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution lists will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Members of the media with questions about the recall can contact Lynne Galia, Corporate Affairs Specialist, Kraft Heinz Foods Company, at lynne.galia@kraftheinz.com. Consumers with questions about the recall can contact The Kraft Heinz Foods Company, Consumer Relations Hotline at (855) 265-7238.

JOLLY TIME® Pop Corn Issues Allergy Alert on Undeclared Milk in Healthy Pop® Kettle Corn 100’s (4 count)

May 14, 2021

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JOLLY TIME Pop Corn today issued a voluntary recall of select Healthy Pop® Kettle Corn 100’s (4 count) because they may contain undeclared milk ingredients. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume the product contained inside the recalled bags.
The products covered by this recall have been regionally distributed to select retailers / warehouses in Arizona, California, Colorado, Idaho, Iowa, Kansas, Minnesota, Missouri, Montana, Nebraska, Nevada, Oregon, South Dakota, Utah, Wisconsin and Wyoming. JOLLY TIME Pop Corn did not distribute these recalled products to any other states.
Retailers    States
Associated Food Stores    Arizona, Colorado, Idaho, Montana,
Nevada, Oregon, Utah, Wyoming
Independent Stores    Colorado, Iowa, Kansas, Minnesota,
Nebraska, South Dakota, Wyoming
Dillon Stores    Kansas, Missouri, Nebraska
Fareway    Iowa (Sergeant Bluff location only)
Ralphs    California
Thiesen Supply Inc.    Iowa, Wisconsin
The specific recalled product information is listed below:
American Pop Corn Company is voluntarily recalling the following JOLLY TIME Healthy Pop® Kettle Corn 100’s (4 count) Microwave Popcorn manufactured on January 25, 2021.
th> 
Product    Item UPC    Production Code    Best By Date
JOLLY TIME Healthy Pop
Kettle Corn 100’s (4 count)    2819000141    1025 (time) 3&4    January 25, 2022
No other JOLLY TIME Pop Corn products, sizes or flavors are recalled.
The recall was initiated after JOLLY TIME was notified by a customer that certain cartons of Healthy Pop Kettle Corn 100’s (4 count) were inadvertently filled with another flavor of popcorn, potentially exposing consumers to undeclared allergen: milk.
No allergic reactions related to this matter have been reported to date. If consumers have an allergy or severe sensitivity to milk, they are encouraged not to consume the product and discard it immediately. JOLLY TIME Pop Corn has informed the FDA of the action.
Consumers with the product noted above can contact JOLLY TIME Pop Corn at 1-712-239-1232 (8 am – 4:45 pm CST, Monday-Friday) or via email at popcorn@jollytime.com.

Global Sanitizers Issues Voluntary Nationwide Recall of Medically Minded Hand Sanitizer Due to Presence of Undeclared Methanol

May 14, 2021

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Las Vegas, NV, Global Sanitizers is voluntarily recalling 50 thousand units of Medically Minded hand sanitizers, lot numbers: E212020 & E082020 Best Buy of 5/21/2022 to the user/consumer level. FDA analysis has found the product to contain methanol.
Risk Statement: Substantial methanol exposure can result in coma, seizures, permanent blindness, permanent damage to the central nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, Global Sanitizers has not received any reports of adverse events related to this recall.
These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. Medically Minded hand sanitizer is packaged in 8.5 oz / 250 ml clear bottles with caps with the following UPC 7675300359. The affected Medically Minded hand sanitizer lots include the following lot numbers and expiration dates E212020 & E082020 Best Buy of 5/21/2022. The product can be identified by the representative label below. The hand sanitizer was distributed Nationwide in the USA to Wholesale companies who further distributed between July 2020 -August 2020.
Global Sanitizers is notifying its distributors and customers by Email, Letter, Telephone & Press Release and is arranging for return of all recalled products. Consumers/distributors/retailers that have Medically Minded hand sanitizer product which is being recalled should stop using/return to place of purchase/discard/contact their doctor.
Consumers with questions regarding this recall can contact Global Sanitizers by calling 702.323.4402 or e-mail address recall@globalsanitizers.com Monday through Friday 9am-5pm pacific standard time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

BUBS Naturals of Encinitas, CA Is Voluntarily Recalling Certain Lots of Its MCT Oil Powder Product Due to Undeclared Milk

May 14, 2021

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BUBS Naturals of Encinitas, CA is voluntarily recalling certain lots of its MCT Oil Powder product because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume this product.
The BUBS Naturals MCT Oil Powder product comes in a 10.6-ounce gusset bag and was distributed through its online store, Amazon, and some grocery stores. The recalled products bear the following lot code and Expiration Date information:
•    BUBS Naturals MCT Oil Powder in Gusset Bags, Lot #’s and Exp dates MCT50200004 Exp. 1/22, MCT50200005 Exp. 1/22, MCT50200006 Exp. 1/22, MCT50200007 Exp. 1/22, MCT50200008 Exp. 1/22, MCT50200009 Exp 1/22, MCT50200010 Exp 1/22, MCT50200011 Exp. 5/22, MCT50200012 Exp. 5/22, MCT50200013 Exp. 5/22; UPC 796752137889
The lot code and expiration date are located on the back of the bag, in bottom center of the panel, as pictured below.
This recall is being initiated because the MCT Oil Powder in this product is under recall for undeclared milk allergens by the ingredient supplier. This recall is being carried out with the knowledge of the Food and Drug Administration.
There have been no reports of illness involving the products addressed in this recall.
Customers with a milk allergy or sensitivity who have purchased the affected product are urged not to consume it and dispose of it or return it to the point of purchase. Consumers with questions regarding this recall can contact BUBS Naturals customer service at info@bubsnaturals.com, 760-456-2631, 9:00 AM – 5:00 PM PST.

Expanded Recall-Scentsational Soaps & Candles, Inc. of Scented Hand Sanitizers Due to the Presence of Methanol (Wood Alcohol), Benzene and Acetaldehyde

May 13, 2021

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Scentsational Soaps & Candles, Inc., has voluntarily expanded its April 27 recall of scented Hand Sanitizers to include three lots of Goose Creek HAND SANITIZER (NDC 75078-004) + Aloe and one lot of COCO TKO HAND SANITIZER in 3.38 and 3.4 fluid ounce spray bottles, respectively, to the consumer level. These products are listed in the table below. These products are being recalled after testing conducted by our firm revealed the presence of methanol (wood alcohol), benzene, and acetaldehyde. These products were sold on the Internet and distributed nationwide in the USA by Goose Creek Candles, LLC and Coconut Stand.
Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest the products and adolescents and adults who drink the products as an alcohol (ethanol) substitute are most at risk for methanol poisoning. Exposure to benzene can occur through inhalation, oral, and skin. There is a reasonable probability that benzene present at levels above the maximum daily exposure recommendations can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. Additionally, animal studies have shown that acetaldehyde can possibly cause cancer in humans. To date, the company has not received any reports of adverse reactions related to this recall.
These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. The affected bottles of hand sanitizer include a five-digit lot code printed on the bottle near the base. The products can be identified by the label, scent, and lot code provided in the table at the end of this release. Photos are also provided at www.scentsational-products.comExternal Link Disclaimer.External Link Disclaimer
Scentsational Soaps & Candles, Inc. has notified its direct customers by telephone with confirmatory email and asked that they remove the recalled products from commerce immediately if they still had any in inventory.
Consumers, distributors, and retailers that have the hand sanitizers which are being recalled should stop using, distributing and/or selling them and return them to the place of purchase.
Consumers with questions regarding this recall can contact our Customer Support Desk, 1-855- 5548050, M-F, during business hours 9:00 a.m. – 5:00 p.m. ET.
Consumers should contact their physician or healthcare provider if they have experienced  problems that may be related to taking or using this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online by regular mail or by fax.
•    Complete and submit the report OnlineExternal Link Disclaimer
•    Regular Mail or Fax: Download formExternal Link Disclaimer or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
“We have discontinued all hand sanitizer production,” said Steve Morrison of Scentsational Soaps & Candles, Inc. “We work hard every day to carefully procure the highest quality ingredients, and we sincerely regret any inconvenience this recall may cause.”  
May 10 2021, Nationwide Hand Sanitizer Spray Recall Voluntarily Initiated by Scentsational Soaps and Candles, Inc.
Label    Scent    Size    UPC or NDC    LOT #
on the side
of the bottle near base    Retailer and States
shipped on 9/22/20
Goose Creek HAND SANITZER + Aloe Goose    Blueberry Limeade Anti-Bacterial Spray    3.38 fl oz. (100 ml)    NO UPC    20258    36 cases shipped on 9/22/20 to KY
Goose Creek HAND SANITIZER + Aloe    Limoncello Anti-Bacterial Spray    3.38 fl oz. (100 ml)    NO UPC    20258    36 cases shipped on 9/22/20 to KY
Goose Creek HAND SANITIZER + Aloe Goose    Beach Dreams Anti-Bacterial Spray    3.38 fl oz. (100 ml)    No UPC    20258    36 cases shipped on 9/22/20 to KY
Goose Creek HAND SANITIZER + Aloe Goose    Grape Soda Anti-Bacterial Spray    3.38 fl oz. (100 ml)    No UPC    20258    36 cases shipped on 9/22/20 to KY
Goose Creek HAND SANITIZER + Aloe Goose    Champagne Bubbles Anti-Bacterial Spray    3.38 fl oz. (100 ml)    No UPC    20258    36 cases shipped on 9/22/20 to KY
Goose Creek HAND SANITIZER + Aloe Goose    Dragonfruit Splash Anti-Bacterial Spray    3.38 fl oz. (100 ml)    No UPC    20258    36 cases shipped on 9/22/20 to KY
Goose Creek HAND SANITIZER + Aloe Goose    Marshmallows Anti-Bacterial Spray    3.38 fl oz. (100 ml)    No UPC    20258    36 cases shipped on 9/22/20 to KY
Goose Creek HAND SANITIZER + Aloe Goose    Melon Picnic Anti-Bacterial Spray    3.38 fl oz. (100 ml)    No UPC    20259    35 cases shipped on 9/22/20 to KY
Goose Creek HAND SANITIZER + Aloe Goose    Optimistic Vibes Anti-Bacterial Spray    3.38 fl oz. (100 ml)    No UPC    20259    36 cases shipped on 9/22/20 to KY
Goose Creek HAND SANITIZER + Aloe Goose    Red White and Blue Anti-Bacterial Spray    3.38 fl oz. (100 ml)    No UPC    20259    42 cases shipped on 9/22/20 to KY
Goose Creek HAND SANITIZER + Aloe Goose    Watermelon Lemonade Anti-Bacterial Spray    3.38 fl oz. (100 ml)    No UPC    20259    35 cases shipped on 9/22/20 to KY
Goose Creek HAND SANITIZER + Aloe Goose    Tropical Daydream Anti-Bacterial Spray    3.38 fl oz. (100 ml)    No UPC    20260    36 cases shipped on 9/22/20 to KY
COCO TKO HAND SANITIZER    Coconut Stand    3.4 fl oz. (100.55 ml)    No UPC    20260    14 cases shipped on 9/16/20 to FL

Dash Xclusive Issues Voluntary Nationwide Recall of Imperia Elita Vitaccino Coffee Due to the Presence of Undeclared Sibutramine and Fluoxetine

May 12, 2021

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Glendale, California, Dash Xclusive is voluntarily recalling all lots of Imperia Elita Vitaccino Coffee to the consumer level. FDA analysis has found the product to contain undeclared sibutramine and fluoxetine. Sibutramine was an FDA-approved drug used as an appetite suppressant for weight loss but was withdrawn from the market because of safety issues, including stroke, heart failure and serious health risk especially to those with underlying heart related disease. Fluoxetine is an FDA approved drug indicated for the treatment of various depressive disorders, obsessive compulsive disorder, bulimia and panic disorders. This drug product carries a box warning for suicidal thoughts and behaviors and it needs to be monitored closely by a prescriber. The presence of sibutramine and fluoxetine in Imperia Elita Vitaccino coffee renders it an unapproved drug for which safety and efficacy has not been established and therefore subject to a recall. Dash Xclusive has not received any reports of adverse events related to this recall.
Risk Statement: Products containing undeclared sibutramine pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. Products containing undeclared fluoxetine could cause suicidal thinking and behavior, an accumulation of high levels of serotonin in the body or neuroleptic malignant syndrome (NMS)-like reactions which is a life-threatening neurological disorder; elevated mood state that can cause higher than normal energy levels, restlessness, decreased need for sleep; abnormal bleeding, and low sodium levels.
The product is marketed  as a dietary supplement for weight loss and is packaged in a black rectangular box and contains fifteen sachets. The affected Imperia Elita Vitaccino coffee lots include all lots. Product was distributed Nationwide in the USA via internet and by ebay at www.ebay.com. On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.
Dash Xclusive is notifying its customers by e-messages on the eBay platform and is arranging for return of all recalled products. Consumers that have Imperia Elita Vitaccino Coffee which is being recalled should stop using/return to Dash Xclusive, 610 S. Verdugo Road, Apt 31, Glendale, California 91205.
Consumers with questions regarding this recall can contact Dash Xclusive by e-mail at dashxclusive11@gmail.com on Mondays to Thursdays from 11am to 4pm Pacific Time zone.  Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online by regular mail or by fax.
•    Complete and submit the report OnlineExternal Link Disclaimer
•    Regular Mail or Fax: Download formExternal Link Disclaimer or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Sara Lee Frozen Bakery Issues Allergy Alert on Undeclared Peanuts in Pecan Pies

May 12, 2021

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Sara Lee Frozen Bakery announced today the recall of specific lots of select Sara Lee, Chef Pierre and Devonshire pecan pies produced between March 4 and April 1, 2021, because the product may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of a serious or life-threatening allergic reaction if they consume the product.
Product was distributed nationwide through food service distributors. Recalled product details are as follows and consumers who believe they have purchased recalled lot codes are urged to confirm the lot code with the place of purchase.
•    Sara Lee Individually Wrapped 4-ounce Pecan Pie slices, 24-count case SKU #5117 produced on March 5, 2021, marked with lot code #C050641C and carrying unit UPC 032100051118. Individual pie slices have a printed lot code on the top of the package.
•    Sara Lee Individually Wrapped 4-ounce Pecan Pie slices, 48-count case SKU #7144 produced on March 4 and March 11, 2021, marked with lot codes #C050631C and #C050701C and carrying unit UPC 032100051118. Individual pie slices have a printed lot code on the top of the package.
•    Chef Pierre 10” Pre-Baked Southern Pecan Pie 36-ounce, case SKU #9273 produced on March 4, 2021, marked with lot code #C040631C and carrying unit UPC 032100092739.
•    Chef Pierre 10” Pre-Baked 10-Slice Pecan Pie 36-ounce, case SKU #9375 produced on April 1, 2021, marked with lot code #C050911C and carrying unit UPC 032100093750.
•    Devonshire Bake Shop 10” Pre-Baked Southern Style Pecan Pie 36-ounce, case SKU #8994 produced on April 1, 2021, marked with lot code #C040911C and carrying unit UPC 758108399877.
There have been no reports of illness or injury to date. This recall has been initiated due to the unintentional cross-contamination of raw pecans in shells with residual peanuts during agricultural transport and storage of pecans by a supplier. Immediate steps were taken to prevent recurrence. Sara Lee Frozen Bakery is conducting this recall with the full knowledge and cooperation of the US Food and Drug Administration.
Sara Lee Frozen Bakery has instructed all impacted distributors to recall and destroy all product in market. Images of the products are attached and available at https://saraleefrozenbakery.com/foodservice/our-products/External Link Disclaimer. Consumers who believe they have purchased recalled lot codes are urged to confirm the lot code with the place of purchase and ask for a full refund if the UPC and lot code matches what is listed above. Consumers with questions may contact the company via email at SaraLeeFrozenBakery@casupport.com or at 1-800-323-7117 between 10am to 6pm EST Monday through Friday.

Natural Way Recalls Almond Butter Due to Undeclared Peanuts

May 7, 2021

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Natural Way of Fayetteville, AR, is recalling its 16 ounce jars of original almond butter because they may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of a serious or life-threatening allergic reaction if they consume the product contained inside the recalled jars.
The recalled almond butter was distributed nationwide in retail stores and through mail orders.
The product comes in a 16 ounce, plastic jars marked with lot #505721 on the bottom and with an almond butter label with a UPC of 850001775175.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after a customer notified Natural Way of a jar of peanut butter mislabeled as almond butter.
Consumers who have purchased 16 ounce jars of Natural Way nut butters are urged to check the UPC and the lot code and return them to the place of purchase for a full refund if the UPC and lot code match what is listed above. Consumers with questions may contact the company at 1-479-595-5660 between 8am-5pm central time Monday through Friday.

Bloommy, Inc Issues Allergy Alert on Undeclared Fish in Bloommy Biotin Collagen Keratin Capsules

May 7, 2021

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Bloommy, Inc. is recalling the following product due to the presence of a fish allergen for the collagen-based ingredient. The best by involved or purchase date prior to 05/04/201.People who have an allergy or severe sensitivity to fish run the risk of serious or life-threatening allergic reaction if they consume these products.
•    Bloommy Biotin Collagen Keratin Capsules for Skin, Joint, and Hair, 60 capsules 
o    Capsule details: 00 clear vegetable capsule
o    Package Dimensions : 3.82 x 2.05 x 2.01 inches; 2.08 Ounces
o    Manufacture Date: 04/2021
o    Best Buy Date: 04/2023
The recalled product was distributed via Amazon through retail orders on product listing https://www.amazon.com/dp/B082PSKMKGExternal Link Disclaimer and online retail website https://mybloommy.com/External Link Disclaimer . A total of 13,688 units were issued out.
No illnesses have been reported to date in connection with this recall/problem.
Bloommy, Inc was notified by the State of Florida regarding this undeclared fish ingredient.
Production of the product will be reissued into circulation with an updated dietary supplement label stating the presence of fish in the fish collagen product of Bloommy Biotin Collagen Keratin Capsules for Skin, Joint, and Hair.
Consumers who have purchased Bloommy Biotin Collagen Keratin Capsules for Skin, Joint, and Hair may contact Bloommy via email email: info@mybloommy.com at +1-860-495-3743 or at 106 W Broad St, Pawcatuck, CT 06379 for any questions, comments or concerns they may have about the product. Contact hours are M-F, 9am to 5pm EST. Customers who have acquired the product and are accustomed to a fish allergy are instructed to throw the product out in their home disposal or public trash and will be issued a refund on the product, preferable email contact is info@mybloommy.com

Arizona Nutritional Supplements Issues Allergy Alert on Undeclared Soy Allergen in 365 Everyday Value Whey Protein Powder Natural Vanilla Flavor

May 7, 2021

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Arizona Nutritional Supplements of Chandler, AZ is voluntarily recalling 13.9 oz. containers of “365 Everyday Value Whey Protein Powder Natural Vanilla Flavor” due to the potential of an undeclared soy allergen. Containers of 365 Everyday Value Whey Protein Powder Natural Vanilla Flavor were mistakenly packaged with Soy Protein Powder resulting in an undeclared Soy allergen. No illnesses have been reported to date.
Individuals with an allergy or sensitivity to soy may risk a serious or life-threatening allergic reaction if they consume this product.
The product can be identified by the UPC 9948228764, a Best By of 03/04/2023 and Lot 0073984. The affected product was sold at Whole Foods Market locations in the United States between March 24, 2021 and May 6, 2021.
Customers who purchased this product at Whole Foods Market can bring a valid receipt into the store for a full refund. Consumers with additional questions can call 1-844-936-8255 between the hours of 7:00 a.m. and 10:00 p.m. CST, Monday through Friday, or 8:00 a.m. and 6:00 p.m. Saturday through Sunday.

Hershey Voluntarily Recalls Hershey’s Chocolate Shell Topping Due to Undeclared Almonds

May 5, 2021

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The Hershey Company (Hershey) today announced a voluntary recall of a single lot of Hershey’s Chocolate Shell Topping in a 7.25-oz. (205g) bottle with UPC (346000) after learning that 1,700 bottles were incorrectly filled with Heath Shell Topping which is made with almonds. Hershey is initiating the voluntary recall to protect public health. People who have an allergy or severe sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume these products.
The products were shipped nationwide between April 15 and May 3, 2021 and bear the product code 25JSAS1. Pictures of the product are included below and are available on www.thehersheycompany.comExternal Link Disclaimer
Hershey’s Chocolate Shell Topping products purchased before April 15, 2021 are not included in this recall. No other  Shell Topping flavors or products distributed by Hershey are involved in this situation.
Hershey has instructed all retailers that received the affected product to immediately remove it from store shelves.
There have been no reports of illness or injury to date. The situation arose due to an isolated error at a contract manufacturing facility. Immediate steps were taken to prevent recurrence. Hershey is conducting this recall with the full knowledge and cooperation of the US Food and Drug Administration.
Consumers who purchased Hershey’s Chocolate Shell Topping products after April 15 with lot code 25JSAS1 should not consume the product and should contact Hershey Consumer Relations for a full refund by calling 1-866-528-6848 Monday through Friday from (9 a.m. to 6 p.m. EST) or visit www.askhershey.comExternal Link Disclaimer.

Frito-Lay Issues Voluntary Allergy Alert on Undeclared Milk In Ruffles All Dressed Potato Chips Distributed Regionally to Sam’s Club

May 5, 2021

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Frito-Lay today issued a voluntary recall of select 16 1/8 oz. bags of Ruffles All DressedPotato Chips because they may contain undeclared milk ingredients. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume the product contained inside the recalled bags.
The products covered by this recall may have been regionally distributed to Sam’s Club warehouses in Alabama, Florida, Georgia, Louisiana, Mississippi, North Carolina, South Carolina, Tennessee, and Virginia. Frito-Lay did not distribute these recalled products to any other retailer.
No other Ruffles products, sizes or flavors are recalled, including bags in Variety Packs.
The recall was initiated after it was discovered that certain bags of Ruffles All Dressed Potato Chips were inadvertently filled with another flavor of potato chips, potentially exposing consumers to undeclared milk.
No allergic reactions related to this matter have been reported to date. If consumers have an allergy or severe sensitivity to milk, they are encouraged not to consume the product and discard it immediately. Frito-Lay has informed the FDA of the action.
Consumers with the product noted above can contact Frito-Lay Consumer Relations at 1-800-352-4477 (9 a.m. – 4:30 p.m. CST, Monday-Friday).
The specific recalled product information is listed below:
Product Description
& Retailer    Size    "UPC Listed on Back of Bag"    Code Date & Manufacturing
Code – Listed on Front of Bag
Along Top Right Side    Representative Image
Ruffles All Dressed Potato Chips
Distributed to Sam’s Club
Warehouses in states listed above    16 1/8 oz.    28400 56520    Both “Guaranteed Fresh” date of
1 JUN 2021
And one of these 9-digit Manufacturing Codes
373205510
473305610
473105610    

Bellisio Foods, Inc. Recalls Beef Pasta Products Due to Misbranding and an Undeclared Allergen

May 4, 2021

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WASHINGTON, May 4, 2021 – Bellisio Foods, Inc., a Jackson, Ohio establishment, is recalling approximately 3,927 pounds of not-ready-to-eat (NRTE) spaghetti with meat sauce product due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains soy, a known allergen, which is not declared on the product label. 
The frozen, NRTE spaghetti with meat sauce items were produced April 22, 2021. The following products are subject to recall:
•    8.5-oz paperboard tray with lid packages containing “Michelina’s Spaghetti with Meat Sauce” with lot code J1112N8, “BEST BY 22APR2022”, and a UPC code of “7 17854 10503 9” on the bottom label.
The product labels can be viewed here. The products subject to recall bear establishment number “EST. 18297” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.                  
The problem was discovered when the company determined soy-containing ingredients may have comingled with the recalled product that does not normally contain soy.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution lists will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers with questions about the recall can contact Krista Cummings, Consumer Affairs, Bellisio Foods, Inc., at (800) 446-5469 or email kcummings@bellisiofoods.com. Members of the media with questions about the recall can contact Tom Lindell, Public Relations, Bellisio Foods, Inc., at (612) 305-6149 or email tom.lindell@exponentpr.com.

Bellisio Foods, Inc. Recalls Beef Pasta Products Due to Misbranding and an Undeclared Allergen

May 4, 2021

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WASHINGTON, May 4, 2021 – Bellisio Foods, Inc., a Jackson, Ohio establishment, is recalling approximately 3,927 pounds of not-ready-to-eat (NRTE) spaghetti with meat sauce product due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains soy, a known allergen, which is not declared on the product label. 
The frozen, NRTE spaghetti with meat sauce items were produced April 22, 2021. The following products are subject to recall:
•    8.5-oz paperboard tray with lid packages containing “Michelina’s Spaghetti with Meat Sauce” with lot code J1112N8, “BEST BY 22APR2022”, and a UPC code of “7 17854 10503 9” on the bottom label.
The product labels can be viewed here. The products subject to recall bear establishment number “EST. 18297” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.                  
The problem was discovered when the company determined soy-containing ingredients may have comingled with the recalled product that does not normally contain soy.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution lists will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers with questions about the recall can contact Krista Cummings, Consumer Affairs, Bellisio Foods, Inc., at (800) 446-5469 or email kcummings@bellisiofoods.com. Members of the media with questions about the recall can contact Tom Lindell, Public Relations, Bellisio Foods, Inc., at (612) 305-6149 or email tom.lindell@exponentpr.com.

Russ Davis Wholesale Issues Allergy Alert on Undeclared Soy in Veggie Pizza

May 4, 2021

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Russ Davis Wholesale of Wadena, Minnesota is voluntarily recalling Veggie Pizza under the Crazy Fresh and Quick & Easy brands as it may contain undeclared soy. People who have an allergy or sever sensitivity to soy run the risk of serious or life-threatening allergic reaction if they consume this product.
Crazy Fresh and Quick & Easy brand Veggie Pizza 6.2 oz, in a clear clam shell, sold in grocery stores located in Iowa, Michigan, Minnesota, North Dakota, South Dakota and Wisconsin. Product with Sell By dates of 04/20/21 through 05/04/21 are impacted by this Recall.
No illnesses have been reported to date.
The recall was initiated after the crust supplier notified Russ Davis of the undeclared soy allergen.
Consumer who purchased Veggie Pizza under the brand of Crazy Fresh or Quick & Easy with soy allergies should not consume this product, and direct questions to Customer Service at 1-877-433-2173.

Evolve Issues Allergy Alert on Undeclared Soy in Vanilla Bean and Double Chocolate 4 Pack Protein Shakes

May 1, 2021

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CytoSport, Inc., the manufacturer of Evolve, today announced a voluntary recall of specific lots of Evolve Protein Shakes after a third-party supplier was found to have supplied ingredients cross-contaminated with soy protein. CytoSport is initiating the voluntary recall to protect public health. Consumers that have an allergy or severe sensitivity to soy run the risk of an allergic reaction if they continue to consume the products.
The products being recalled were distributed nationwide through retailers, eCommerce websites and through the www.drinkevolve.comExternal Link Disclaimer website, and are as follows:
Product    Package    MFG Date
Evolve Double Chocolate Protein Shake    11 oz - Tetra Pak cartons sold in 4 pack    12/31/2020
Evolve Double Chocolate Protein Shake    11 oz - Tetra Pak cartons sold in 4 pack    1/1/2021
Evolve Vanilla Bean Protein Shake    11 oz - Tetra Pak cartons sold in 4 pack    12/30/2020
Evolve Vanilla Bean Protein Shake    11 oz - Tetra Pak cartons sold in 4 pack    1/25/2021
Pictures of the products listed above will be available on www.drinkevolve.comExternal Link Disclaimer. There have been no reported illnesses to date.
At this time there are no other Evolve products involved in this situation. All retail outlets effected have been notified to immediately remove effected product from shelves. The company is working closely with the Food and Drug Administration (FDA) and has rectified the issue, but in the meantime is taking these actions out of commitment to and concern for consumers.
Consumers who have purchased any of the above products are urged to dispose of or return them to the place of purchase for a full refund. They may also call CytoSport Customer Relations at 1-888-298-6629 Monday through Friday from 9:00 am to 5pm EST.

Hempstead Foodservice Recalls Pork Products Due to Misbranding and Undeclared Allergens

May 1, 2021

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WASHINGTON, May 1, 2021 – Hempstead Foodservice, a Hempstead, N.Y. establishment, is recalling approximately 972 pounds of pork chop products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains hydrolyzed soy protein, a known allergen, which is not declared on the product label. 
The heat-treated fresh pork chop items were produced on various dates between April 6, 2021 and April 30, 2021. The following products are subject to recall:
•    10-41 lb. carboard boxes containing the product in clear plastic bags with “Hempstead Foodservice” on the box and “PORK CHOPS” marked from the list on the side of the box.
Refer to the link here for additional product information. The products subject to recall bear establishment number “EST. 47142” inside the USDA mark of inspection. These items were shipped to grocery stores and restaurants in New York. The products are cooked at these retailers and then further sold to consumers.
The problem was discovered through routine FSIS verification activities.  
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
FSIS is concerned that some product may be in retailer and consumers’ refrigerators. Retailers who have obtained these products are urged not to sell them. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. Any consumers concerned about a cooked or prepared pork chop product they recently purchased should contact the store for further details.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
Consumers and members of the media with questions about the recall can contact Edgar Puello, Owner, Hempstead Foodservice at (516) 385-1212 or email info@hempsteadfoodservice.com.

Scentsational Soaps & Candles, Inc. Issues Voluntary Nationwide Recall of Scented Hand Sanitizers Due to the Presence of Methanol (Wood Alcohol), Benzene and Acetaldehyde

April 30, 2021

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Scentsational Soaps & Candles, Inc., is voluntarily recalling 5 lots of Scentsational Soaps & Candles scented Hand Sanitizers from the Black and White Collection and Photo Real Collection and 3 lots of Ulta Beauty Collection scented Hand Sanitizer Spray packaged in 3.38 and 3.4 fluid ounce spray bottles, respectively, to the consumer level. See products listed in the table below. These products are being recalled after testing conducted by our firm revealed the presence of methanol (wood alcohol), benzene, and acetaldehyde. These products were distributed nationwide in the USA through Ulta Beauty, TJ Maxx, and Marshalls retail stores.
Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest the products and adolescents and adults who drink the products as an alcohol (ethanol) substitute are most at risk for methanol poisoning. Exposure to benzene can occur through inhalation, oral, and skin. There is a reasonable probability that benzene present at levels above the maximum daily exposure recommendations can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be lifethreatening. Additionally, animal studies have shown that acetaldehyde can possibly cause cancer in humans. To date, the company has not received any reports of adverse reactions related to this recall.
These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. The affected bottles of hand sanitizer include a five-digit lot code printed on the bottle near the base or, in the case of the Ulta Beauty Collection product, a five-digit lot code followed by a single letter. The products can be identified by the label, scent, and lot code provided in the table at the end of this release. Photos are also provided at www.scentsational-products.comExternal Link Disclaimer.External Link Disclaimer
Scentsational Soaps & Candles, Inc., has notified its direct customers by telephone with confirmatory email and asked that they remove the recalled products from commerce immediately if they still had any in inventory.
Consumers, distributors and retailers that have the hand sanitizers which are being recalled should stop using, distributing and/or selling them and return them to the place of purchase.  Ulta Beauty has confirmed it has removed the recalled Ulta Beauty Collection product from its stores and online.
Consumers with questions regarding this recall can contact our Customer Support Desk, 1-855-554-8050, M-F, during business hours 9:00 a.m. – 5:00 p.m. ET.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
“As the owners of the company, my wife and I want to reassure consumers and our customers that we are doing absolutely everything possible to carry out this recall efficiently and effectively and ensure it does not happen again.” said Steve Morrison of Scentsational Soaps & Candles, Inc.
Label    Scent    Size    UPC    LOT #    Retailer and States
Ulta Beauty Collection    Fresh Lemon Scented Hand Sanitizer    100.55ml/3.4 fl. oz.    717897092017    20357A, 20358B, 20363C    Ulta Beauty: CA, IL, IN, PA, TX
SS Black and White Collection    Coconut Breeze Black and White Hand Sanitizer    3.38 FL.OZ. (100mL)    NO UPC    20252    TJ Maxx: IN, MA, NC, NV, TX
Marshalls: AZ, GA, MA
SS Black and White Collection    Eucalyptus & Mint Black and White Hand Sanitizer    3.38 FL.OZ. (100mL)    NO UPC    20248    TJ Maxx: IN, MA, NC, NV, TX
Marshalls: AZ, MA, VA
SS Black and White Collection    Lavender & Herbs Black and White Hand Sanitizer    3.38 FL.OZ. (100mL)    NO UPC    20253    TJ Maxx: IN, MA, NC, NV, TX
Marshalls: AZ, GA, MA, VA
SS Black and White Collection    Lemon Zest Black and White Hand Sanitizer    3.38 FL.OZ. (100mL)    NO UPC    20255    TJ Maxx: IN, MA, NC, NV, TX
Marshalls: AZ, MA, VA
SS Black and White Collection    SS Tangerine & Guava Black and White Hand Sanitizer    3.38 FL.OZ.(100mL)    NO UPC    20254    TJ Maxx: IN, MA, NC, NV, TX
Marshalls: AZ, GA, MA
SS Photo Real Collection    Coconut Breeze Photo Real Hand Sanitizer    3.38 FL.OZ.(100mL)    NO UPC    20252    TJ Maxx: IN, MA, NC, NV, TX
Marshalls: AZ, GA, MA
SS Photo Real Collection    Eucalyptus & Mint Photo Real Hand Sanitizer    3.38 FL.OZ.(100mL)    NO UPC    20248    TJ Maxx: IN, MA, NC, NV, TX
Marshalls: AZ, MA, VA
SS Photo Real Collection    Lavender & Herbs Photo RealHand Sanitizer    3.38 FL.OZ.(100mL)    NO UPC    20252    TJ Maxx: IN, MA, NC, NV, TX
Marshalls: AZ, GA, MA, VA
SS Photo Real Collection    Lemon Zest Photo Real Hand Sanitizer    3.38 FL.OZ.(100mL)    NO UPC    20255    TJ Maxx: IN, MA, NC, NV, TX
Marshalls: AZ, GA, MA, VA
SS Photo Real Collection    Tangerine & Guava Photo Real Hand Sanitizer    3.38 FL.OZ.(100mL)    NO UPC    20254    TJ Maxx: IN, MA, NC, NV, TX
Marshalls: AZ, MA, VA

More Than Gourmet, Inc. Recalls Beef And Veal Broth And Stock Products Due To Possible Foreign Matter Contamination

April 30, 2021

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WASHINGTON, April 24, 2021– More Than Gourmet, Inc., an Akron, Ohio establishment, is recalling approximately 6,896 pounds of ready-to-eat beef and veal broth and stock products that may be contaminated with extraneous materials, specifically hydraulic oil, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The ready-to-eat broth and stock items were produced on March 1, 2021, April 7, 2021 and April 8, 2021. The following products are subject to recall: [View Labels (PDF Only)]:
•    12-oz plastic squeeze bottle of KITCHEN ACCOMPLICE ORGANIC Beef BONE BROTH Concentrate and lot code MFGA21060A5613, MFGA21060B5613 & MFGA21098B5613 with Use by/Sell by date of 3/1/2023 & 4/8/2023.
•    16-oz. plastic cup of MORE THAN GOURMET Demi-Glace Gold CLASSIC FRENCH DEMI-GLACE and lot code MFGA21097A0205 with Use by/Sell by date of 4/7/2023.
The products subject to recall bear establishment number “27446” inside the USDA mark of inspection. These items were shipped to retailers and distributors nationwide.     
The problem was discovered by the establishment after identifying a malfunction in a piece of processing equipment.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
Consumers with questions about the recall can contact More Than Gourmet, Inc. customer service at 800-860-9391 and sales@morethangourmet.com and members of the media can contact Paul Taylor, Vice President at 330-762-6652.

Basic Grain Products, Inc. Issues Allergen Alert on Undeclared Milk in Caramel Rice Cakes

April 28, 2021

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Basic Grain Products, Inc. in Coldwater, Ohio, is voluntarily recalling 6.56-ounce bags of Kroger and Stop & Shop brand’s Caramel Rice Cakes because they may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume this product. Individuals exhibiting signs or symptoms of foodborne illness or allergies should contact a physician immediately.
The product comes in a 6.5-ounce bag. The Best if Used By or Best Before date (also the Lot Code) is located on the plastic Kwik Lok tag at the top of the bag. Only two lots of the product are affected. The recalled packages bear the following UPC and lot code information:
•    Kroger Caramel Rice Cakes, UPC 0 11110 35792 2, Best if Used By dates DEC1521 and DEC1621, shipped to retail distribution centers in CO, IN and KS. (photos provided below)
•    Stop & Shop Caramel Rice Cakes, UPC 6 88267 07615 2, Best Before date DEC1521, shipped to retail distribution centers in CT and PA. (photos provided below)
The undeclared milk was discovered by internal control systems. This recall is being carried out with the knowledge of the U.S. Food and Drug Administration.
To date, there have been no reports of illness involving products addressed in this recall.
Customers with a milk allergy or sensitivity who have purchased the affected product are urged not to consume it and dispose of it or return it to the point of purchase. Consumers with questions regarding this recall can contact Basic Grain Products’ customer service desk at recall@basicgrain.com, 1-888-386-2075 M-F, 9:00 a.m. – 5:00 p.m. EST.

Velvet Ice Cream Recalls Various Products Due to Possible Listeria Risk

April 27, 2021

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Velvet Ice Cream has announced it is voluntarily recalling all of its ice cream and sherbet products made on or after March 24, 2021 as a precaution because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.
Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
No illness or injury has been associated with the recalled products, which are being recalled in cooperation with the U.S. Food and Drug Administration. The issue was identified as a result of the company’s routine testing.
The products were distributed to Indiana, Kentucky, Ohio, and West Virginia through various drug stores, convenience stores and supermarkets. They are packaged in various sizes and containers.
The products were distributed and sold in supermarkets from on or after March 24, 2021 with the following product codes, which can be found at the bottom or side of the container:
Product Code    Item Description
21104    Buehler’s Chocolate Pail
21104    Buehler’s Neapolitan Pail
21104    Buehler’s Vanilla Pail
21089    Discount Drug Mart Chocolate Swirl Pail
21106    Discount Drug Mart Neapolitan 56oz
21095    Discount Drug Mart Strawberry 56
21091    Discount Drug Mart Vanilla 56
21083    Discount Drug Mart Vanilla Pail
21096    North Star Frog Spit
21097    North Star Frog Spit
21098    North Star Frog Spit
21099    North Star Frog Spit
21089    Whale of a Pail Chocolate Fudge Pai
21090    Whale of a Pail Cookies n Cream
21104    Whale of a Pail Neapolitan
21103    Ruggle’s Orange Sherbet Quarts
21104    Whale of a Pail Vanilla Chocolate
21089    Whale of a Pail Vanilla
Product Code    Item Description
21090    Whale of a Pail Vanilla
21090    Super Dip Chocolate Pail
21103    Super Dip Chocolate Swirl Pail
21083    Super Dip Chocolate Swirl Pail
21089    Super Dip Chocolate Swirl Pail
21083    Super Dip Cookie n Cream Pail
21106    Super Dip Neapolitan 56oz
21104    Super Dip Neapolitan Pail
21095    Super Dip Strawberry 56
21106    Super Dip Superfriends 56oz
21091    Super Dip Vanilla 56
21083    Super Dip Vanilla Pail
21103    Super Dip Vanilla Pail
21089    Super Dip Vanilla Pail
21090    Super Dip Vanilla Pail
21106    Super Dip Vanilla/Orange 56oz
21106    Velvet erVanilla Lovers Trio 56oz
21091    Velvet Banana Cream Pie 56
21088    Velvet Birthday Cake 3 gallon
21084    Velvet Black Walnut 3 gallon
21099    Velvet Blackberry Cobbler 56
21095    Velvet Blueberry Cheesecake 56
21095    Velvet Buckeye Brownie 56
21091    Velvet Buckeye Brownie 56
21095    Velvet Buckeye Classic 56
21096    Velvet Buckeye Classic Pint
21102    Velvet Buckeye Sandwich 12/10pk
21096    Velvet Butter Pecan & Cashew Pint
21105    Velvet Campfire Smores 56oz
21100    Velvet Caramel Pecan 56
21106    Velvet Chocolate Pint
21096    Velvet Chocolate Pint
21105    Velvet Cookie Dough Extreme 56oz
21105    Velvet Cookie Dough Extreme 3 gallon
21084    Velvet Cookie n Cream 3 gallon
21092    Velvet Cookies n Cream Pint
21103    Velvet Cotton Candy 3 gallon
21092    Velvet Dutch Chocolate 56
21089    Velvet Dutch Chocolate 3 gallon
21102    Velvet Dutch Chocolate 3 gallon
21099    Velvet Elephant Ear 56
21084    Velvet Elephant Ear 3 gallon
Product Code    Item Description
21092    Velvet Homemade Vanilla 56
21105    Velvet Homemade Vanilla 56oz
21100    Velvet Kentucky Praline Pecan 56
21085    Velvet Lime Sherbet Quart
21103    Velvet Lime Sherbet Quarts
21091    Velvet Mint Chocolate Chip 56
21102    Velvet Mint Chocolate Chip 3 gallon
21091    Velvet Moose Tracks 56
21095    Velvet Moose Tracks 56
21096    Velvet Moose Tracks Pint
21092    Velvet Olde Tyme Vanilla 56
21105    Velvet Olde Tyme Vanilla 56oz
21102    Velvet Olde Tyme Vanilla 3 gallon
21084    Velvet Orange Sherbet 3 gallon
21085    Velvet Orange Sherbet Quart
21103    Velvet Orange Sherbet Quarts
21091    Velvet Original Vanilla 56
21084    Velvet Original Vanilla 3 gallon
21089    Velvet Original Vanilla 3 gallon
21100    Velvet Original Vanilla 3 gallon
21102    Velvet Original Vanilla 3 gallon
21084    Velvet Pineapple Sherbet 3 gallon
21084    Velvet Pineapple Sherbet Quart
21085    Velvet Pineapple Sherbet Quart
21103    Velvet Pineapple Sherbet Quarts
21103    Velvet Rainbow Sherbet 3 gallon
21103    Velvet Rainbow Sherbet Quarts
21085    Velvet Raspberry Sherbet Quart
21084    Velvet Sea Salt Caramel Toffee 3 gallon
21099    Velvet Summertime Peach 56
21099    Velvet Summertime Peach 3 gallon
21084    Velvet Summertime Peach 3 gallon
21092    Velvet Triple Chocolate Chunk 56
21100    Velvet Vanilla Bean 3 gallon
21088    Velvet Vanilla Pint
21106    Velvet Vanilla Pint
“We’re conducting this voluntary recall in cooperation with the FDA out of consideration for the wellbeing and safety of our customers and consumers,” said Velvet Ice Cream CEO Luconda Dager. “We continue to be committed to serving consumers with high quality ice cream and sherbet products.”
Anyone who has the recalled product in their possession should dispose of it immediately or return it to the place of purchase for a refund. Consumers with questions may contact Velvet Ice Cream at 800-589-5000 x237 from 8 a.m. to 5 p.m. EST, Monday through Friday. Or visit its website at www.velveticecream.com/contact-usExternal Link Disclaimer.

Super World Trading Inc. Recalls Ineligible Ready-To-Eat Siluriformes Products Imported From China

April 23, 2021

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WASHINGTON, April 23, 2021 – Super World Trading Inc., a Brooklyn, N.Y. establishment, is recalling approximately 26,270 pounds of ready-to-eat (RTE) imported Siluriformes products. The products were imported from the People’s Republic of China, a country ineligible to export processed Siluriformes products to the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. 
The following products are subject to recall, regardless of the product date: 
•    4.23 oz. (120g) plastic tray and cover packages containing “Golden Spoon Hot Pot Fish Chips”.
Refer to the label link here for additional product information. The products do not bear an establishment number nor a USDA mark of inspection. These items were shipped to retail and wholesale locations nationwide.
The problem was discovered during a routine FSIS surveillance activity of imported products. China is eligible to import raw Siluriformes products into the United States, but not processed or RTE Siluriformes products.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.  
FSIS is concerned that consumers may still be in possession of the product. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Ling Cho, Admin Asst., Super World Trading Inc., at (718) 381-5659 or email superworldtrading@yahoo.com.

Wolfies Roasted Nut Co. Issues Voluntary Recall of its Crunchy Cheddar & Jalapeno Nuts

April 23, 2021

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Wolfies Roasted Nut Co. in Findlay, Ohio is voluntarily recalling its Crunchy Cheddar & Jalapeno Nuts due to an undeclared milk allergen. This recall has been initiated due to the ingredient label not stating a milk allergen. Products were packaged in either a 5 oz, 14 oz, 28 oz black rice paper stand up pouch or an 80 oz clear poly bag labeled “Cheddar & Jalapeno” with a Wolfies Roasted Nuts label. Products were available for sale at the following locations in Ohio:
•    Wolfies Roasted Nuts & Deli, Findlay
•    Another Wolfies, Findlay
•    Southside Wolfies, Findlay
•    Brinkman’s Country Corner, Findlay
•    Great Scot Supermarkets, Findlay (both locations)
•    Dietsch Brothers, Findlay (both locations)
•    Bowling Green Beer Works, Bowling Green
•    Brooky’s Express, Ottawa
•    Cigars N Stuff, Findlay
•    Coffee Amici, Findlay
•    Continental Plaza, Wauseon
•    Homestead Collection, Findlay
•    Hometown Market Place, Carey
•    Millers Meats, Findlay
•    Moose Lodge #698, Findlay
•    Smoke-N-Stuff, Findlay
•    West End Tavern, Findlay
•    West Side Carryout, Findlay
The issue was discovered during a routine inspection conducted by the Food & Drug Administration (FDA). There have been no reports of illness involving products addressed in this recall; however, people who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume this product. Individuals exhibiting signs or symptoms of food-borne illness or allergies should contact a physician immediately.
Customers with a milk allergy or sensitivity who have purchased the affected product should dispose of it or return it to Wolfies Roasted Nut Co. for a replacement. Consumers with questions regarding this recall can contact Wolfies Roasted Nut Co. at 419-423-1355.

Guan’s Mushroom Co Recalls Enoki Because of Possible Health Risk

April 20, 2021

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Guan’s Mushroom Co of Commerce, CA is recalling all cases of its 200g/7.05-ounce packages of Enoki Mushroom (Product of China) because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.  Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled products were distributed from CA, NY, PA through produce distributors or wholesalers to retail stores nationwide.
The Enoki comes in a 200g/7.05ounces, clear plastic package with the description “Enoki Mushroom” in English, Korean and French, and Guan’s logo in the front.  At the back, there is UPC code: 810023170303.  Product code is RY3428A or RY3434A in the front bottom.
The product is being shipped in a white cardboard box with 25 pcs of 200g.  The box contains Guan’s logo in blue color and product code RY3428A or RY3434A.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after routine testing by Michigan Department of Agriculture and Rural Development revealed the presence of Listeria monocytogenes in 200g package of Enoki.
The distribution of the product has been suspended.
Consumers who have purchased 200g packages of Enoki are urged to return them to the place of purchase for a full refund.  Consumers with question may contact the company at 323.223.1188. 

Creative Foods Inc Issues Allergy Alert on Undeclared Hazelnut, Peanut And Barley (Gluten) In Two Coffee Substitute Gluten-Free Products

April 17, 2021

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Creative Foods Inc. of Prineville, Oregon is recalling two products, Bueno Coffee Substitute Creamy Hazelnut and Bueno Coffee Substitute Pecan Praline. They both may contain undeclared peanut, hazelnut, and/or barley (gluten). While any gluten-containing product can cause health problems for individuals with celiac disease and other gluten sensitivities. People who have hazelnut or peanut allergy run a risk of serious or life-threatening allergic reaction if they consume these products.
Bueno Coffee Substitute Creamy Hazelnut product contains undeclared peanut and hazelnut. Bueno Coffee Substitute Pecan Praline product contains undeclared peanut and barley (which contains gluten). We are recalling all products that have a sell by date of April 8, 2023 or earlier.
Both products have been distributed to stores nationwide for more than 20 years, with the last distribution date of April 8, 2021.
The Bueno Coffee Creamy Hazelnut, UPC 679345100203, is in a matt/white gusseted coffee bag that is 9” tall by 3” wide by 2” deep. It contains 7 ounces of product. The front label has a coffee cup with the brand name Bueno Coffee on the front. The top of the label says, “Bueno Coffee Substitute”, smaller letters under this say, “Garbanzo Coffee”. The back label falsely declares that the product is gluten free and the ingredient list declares “Just Garbanzo Beans (Chickpeas) and natural hazelnut flavoring”.
The Bueno Coffee Creamy Pecan Praline, UPC 679345100104, is in a brown kraft gusseted coffee bag with a purple label. It is 9” tall by 3” wide by 2” deep and contains 7 ounces of product. On the front label it has a coffee cup with the brand name Bueno Coffee. The top of the label says, “Bueno Coffee Substitute”, smaller letters under this say, “Garbanzo Coffee”. In the middle of the label the product flavor “Pecan Praline” is displayed. The back label falsely declares that the product is gluten free and the ingredient list declares “Simply garbanzo beans and natural flavoring”.
No illnesses have been reported to date.
The recall was initiated after it was discovered that Coffee Substitute Gluten-Free products containing hazelnut, peanut and barley (gluten containing grain) were distributed in packaging that did not reveal the presence of these allergens.
This recall is being made with the knowledge of the U.S. Food and Drug Administration and the Oregon Department of Agriculture.
Consumers who have hazelnut or peanut allergy or are sensitive to gluten are urged not to consume the recalled products and should return it to the place of purchase for a full refund.
Consumers with questions may contact the company via email at buenocoffee@gmail.com or call 541-788-2836, 9 am-4:00 pm PST, Monday-Friday.

Jule’s Foods Issues Voluntary Recall of Jule’s Foods Products Because of Possible Health Risk

April 22, 2021

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Jule’s Foods of Carlsbad, CA is voluntarily recalling all Jule’s Foods products, because the product was potentially contaminated with Salmonella.
Products include:
Jule’s Cashew Brie (Classic)
UPC: 860388001507 - all expiration dates
Jule’s Truffle Cashew Brie
UPC: 860388001514 - all expiration dates
Jule’s Black Garlic Cashew Brie
UPC: 860388001552 - all expiration dates
Jule’s Artichoke Spinach Dip
UPC: 860388001569 - all expiration dates
Jule’s Vegan Ranch Dressing
UPC: 860388001521 - all expiration dates
To date, FDA has preliminary confirmation of Salmonella in brie products containing cashews. We are working with the FDA to isolate the source of the pathogen in samples which were collected by the California Department of Public Health. Jule's Foods is issuing this recall in connection with a Salmonella outbreak under investigation by the FDA and CDC.
Products were distributed to primarily independently owned grocery stores in Arkansas, California, Colorado, Connecticut, Florida, Louisiana, Maryland, Minnesota, Nevada New York, New Jersey, Ohio, Oregon, Pennsylvania, Rhode Island, Tennessee, Texas as well as direct to consumer. Jule’s Foods Brie products are 6 ounces and wrapped in white cheese paper. A full list of stores is available at www.JulesFoods.netExternal Link Disclaimer.
Consumption of food contaminated with Salmonella can cause salmonellosis. The most common symptoms of salmonellosis are diarrhea, abdominal cramps, and fever within 12 to 72 hours after eating a contaminated product. Most people recover without treatment. In rare circumstances, infection can produce more severe illness and require hospitalization. Older adults, infants, and persons with weakened immune systems are more likely to develop a severe illness. Individuals concerned about an illness should contact their health care provider.
Production of these products has been suspended while the FDA and the company continue their investigation as to the source of the problem.
Please do not consume the product and immediately dispose of the product or return to the place of purchase for a full refund.
Consumers with questions may contact the company via email at jules@julesveganfoods.com or telephone at (310) 980-4697 between 9 a.m. – 5 p.m. PDT.

Lake Champlain Chocolates Voluntarily Recalls Mr. Goodtime Bunny With Best By Date 11/20/2021 for Undeclared Almonds

April 15, 2021

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Lake Champlain Chocolates (LCC) is issuing a public alert and a voluntary recall on a mis-labeled Mr. Goodtime Bunny with a Best By date of 11/20/21 that may have been purchased between 2/22/21-3/25/21. LCC is issuing this recall after a consumer reported that the product contained almonds, which were not declared on the label.
Any consumer who has a known nut allergy and purchased the Mr. Goodtime Bunny with a Best By date of 11/20/21 should not consume this product. People who have an allergy or severe sensitivity to almonds run the risk of serious or a life-threatening allergic reaction if they consume this product. Consumers with a mislabeled bunny may request a replacement. To date, no consumers have reported injuries or illnesses.
This product was distributed through 16 retailers in 9 states, through the company’s website and its 750 Pine Street Retail Store in Burlington, Vermont. Affected states include: CA, CT, MA, NH, NY, RI, TX, VT, VA.
Affected items detail:
Only customers who purchased a bunny that looks like the image in the link below with the corresponding label are affected by this recall.
The Country Bunny Basket may contain the affected bunny. See below for image of the Country Bunny Basket.
The FDA has been informed of this voluntary recall and will post this notice on their website.
Lake Champlain Chocolates is committed to quality products and consumer safety and is taking aggressive corrective action to prevent the need for any future recalls of its products. It emphasizes that no other LCC products or batch codes were affected.
Lake Champlain Chocolates apologizes for any inconvenience to its customers. Customer service will be available 8:30am-5pm, EST, Monday-Friday to answer any questions regarding this recall.

Church & Dwight Initiates Voluntary Recall of Select Vitamins Due to Isolated Manufacturing Issue

April 20, 2021

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EWING, N.J – Church & Dwight Co., Inc. (NYSE:CHD) initiated a voluntary recall of select vitafusion gummy products after the Company’s investigation of two consumer reports identified the possible presence of a metallic mesh material in product lots manufactured in a four-day period between October 29 and November 3, 2020. The Company is not aware of any reports of consumer illness or injury to-date. In some severe cases, ingesting a metallic material could lead to damage of the digestive tract.
Church & Dwight is coordinating closely with the U.S. Food & Drug Administration (FDA) and following all relevant protocols. The recalled gummy vitamin products are listed below with the Universal Product Code (UPC) and Lot Code. No other products are included in this recall. These products were distributed to in-store and e-commerce retailers from November 13, 2020 through April 9, 2021.
Consumers who have purchased one of the products listed below should stop consumption immediately. Please call our dedicated Consumer Affairs team at +1 (800) 981-4710 before disposing of the product, and we will provide a full refund. Any additional questions can also be directed to our Consumer Affairs team Monday through Friday, 9am – 5pm ET. In the event of illness or injury, consumers can contact Safety Call at +1 (888) 234-1828.
RECALLED PRODUCT LIST
Reference to identify affected plastic bottled gummy vitamin products via Universal Product Code (UPC) and Lot Code.
How to identify affected product UPC and Lot Code.
Church & Dwight Co., Inc. founded in 1846, is located in Ewing, New Jersey. For more information, visit the Company’s website at ChurchDwight.comExternal Link Disclaimer.

Shearer’s Foods LLC Issues Allergy Alert on Undeclared Milk in Raley’s Salt & Vinegar Flavored Potato Chips

April 19, 2021

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Shearer’s Foods LLC of Massillon, OH is voluntarily recalling two lots of 9.5 ounce bags of “Raley’s Salt & Vinegar Flavored Potato Chips,” because they may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume this product.
Raley’s Salt & Vinegar Flavored Potato Chips were distributed at Raley’s retail stores in: CA
The product comes in a 9.5 ounce bag. Only two lots of the product are affected. The recalled packages bear the following UPC and Sell By”/lot code information:
UPC 10046567025466
Sell By    Sell By
08 2 21
06109805    05 17 21
06102005
There have been no reports of illness.
This recall is being made with the knowledge of the U.S. Food and Drug Administration.
Consumers who have purchased 9.5 ounce packaged of Raley’s Salt & Vinegar Flavored Potato Chips with the “Sell By” dates at issue are urged not to eat the product and to return it to the store for a full refund. Consumers with questions may contact a Shearer’s representative Monday through Friday from 8:30am – 4:30pm EST at 1-800-428-6843.

Durisan Announces a Voluntary Recall Expansion of its Antimicrobial Hand Sanitizer

April 16, 2021

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Sanit Technologies LLC d/b/a Durisan announces a voluntary recall expansion of its Durisan Antimicrobial Hand Sanitizer, NonAlcohol products in various sizes listed to now include products that have not yet expired. The products are being recalled due to out of specification microbial contamination. The issue was discovered during a routine audit.
To date, no reports of adverse reactions or customer complaints have been reported related to this recall.
The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available.
Use of a hand sanitizer contaminated with Burkholderia contaminans, generally considered to be of low virulence, can range from no reaction to possible infections in a person with a hand wound or scrapes because the bacteria could enter the bloodstream, especially in patients with compromised immune systems.
The product is packaged in sizes ranging from 18mL credit cards, to bottles sized in 118, 236, 300 and 550 mL and 1000mL wall mounted dispenser refills. 
Durisan Antimicrobial Solutions Hand Sanitizer Sizes With the Following Identification
Volume mL    Volume oz.    UPC    NDC
18    0.61    8 52379 00614 1    71120-112-01
118    4    8 52379 00634 9    71120-112-10
236    8    8 52379 00635 6    71120-112-11
300    10    8 52379 00697 4    71120-112-08
550    18.59    8 52379 00620 2    71120-112-06
1000    33.81    8 52379 00610 3    71120-112-05
The list of the lot numbers of the subject products, which have a 24-month expiration, is included in the link below.
Durisan has provided written notification to its distributors and retailers and is alerting customers via this voluntary recall. Consumers that have the product are advised to contact Durisan to return it.
Consumers with questions regarding this recall can contact Durisan at 941-351-9114, 8:30 am - 4:30 pm Eastern time, Monday through Friday or by email at customerservice@durisan.com.

Blount Fine Foods Voluntarily Recalls a Limited Amount (a Single Lot) of Lobster Bisque Due to Possible Undeclared Egg Allergen

April 16, 2021

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Blount Fine Foods announced that, in partnership with the FDA, it is voluntarily recalling a limited amount (a single lot—2,987 cases total) of 16 oz. Panera at Home Lobster Bisque due to potential contamination with an undeclared egg allergen. The recall is limited to 1 SKU of 16 oz. Panera at Home Lobster Bisque cups produced with lot number 030821-11K and “Use By” date of 5/17/2021. This item is only sold in refrigerated cases in the deli department of grocery-retail stores; it is NOT sold at any Panera bakery-cafe.
This voluntary recall is limited only to 16 oz. Panera at Home Lobster Bisque. No other Panera Bread, Panera at Home or Blount products are affected by this voluntary recall. No illness complaints have been reported to date in connection with this recall. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reactions if they consume this product.
The recalled product is listed below. Consumers can find lot number and “Use By” date on the bottom of each package.
UPC Code    Item    “Use By” Date    Lot Number
077958690300    Panera Lobster Bisque, 16oz    5/17/2021    030821-11K
A limited quantity of this product was distributed across 20 states which include: CA, CO, GA, IL, IN, KS, MA, MD, MI, MO, NC, NE, NJ, OK, OR, PA, TX, VA, WA, WI.
Consumers can contact Blount Fine Foods Customer Care at 1-866-674-4519 for additional information Monday – Friday from 9 AM to 9 PM Eastern Standard Time. Additionally, consumers who have purchased the specific recalled product are urged to return it to the place of purchase or visit www.blountfinefoods.com/recallExternal Link Disclaimer for product reimbursement.

Jose Madrid Salsa Issues a Voluntary Recall Due to an Undeclared Anchovy Allergen

April 16, 2021

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Jose Madrid Salsa in Zanesville, Ohio is voluntarily recalling its Strawberry Mild salsa, packaged in 13oz glass jars, due to an undeclared anchovy allergen.  
Products were available for sale from 3/26/2018-3/29/2021 at farmers markets, josemadridsalsa.comExternal Link Disclaimer and at the following retail locations:
Collins Greenhouse, Mount Vernon, OH    Oberlin IGA, Oberlin, OH
Cornell’s Foods, Huron, OH    Prater’s Highway Market, Adams Mills, OH
Edinberg Corner Store, Rootstown, OH    Ridgewood General Store, West Lafayette, OH
Fields Grocery, West Mansfield, OH    Sweet Berry Fresh Market, Wickliffe, OH
Lancaster Greenhouse, Lancaster, OH    Weiland’s Market, Columbus, OH
Maser’s Farm Market, Powell, OH    Zagara’s Marketplace, Cleveland Hts, OH
The issue was discovered during a routine inspection conducted by the Ohio Department of Agriculture. There have been no reports of illness involving the product addressed in this recall, however, people who have an allergy or severe sensitivity to anchovy run the risk of a serious or life-threatening allergic reaction if they consume this product. Individuals exhibiting signs or symptoms of foodborne illness or allergies should contact a physician immediately.
Customers with an anchovy allergy or sensitivity who have purchased the affected product should dispose of it immediately and contact Jose Madrid Salsa for a replacement jar. Consumers with questions regarding this recall can contact Matthew Harlin at 740-521-4304.

JBS USA Food Company Recalls Imported Boneless Beef Products Due to Possible E. coli O157:H7 Contamination

April 16, 2021

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WASHINGTON, April 16, 2021 – JBS USA Food Company, a Greeley, Colo. firm and Importer of Record, is recalling approximately 4,860 pounds of imported boneless beef products that may be contaminated with E. coli O157:H7, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The raw, frozen, boneless beef products were imported on or around Nov. 10, 2020 and distributed for further processing. The following products are subject to recall [View Label (PDF Only)]:
•    60-lb. cardboard boxes containing “95CL BONELESS BEEF PRODUCT OF AUSTRALIA” with “PACKED ON: 02-SEP-20” and Australian “EST. 4” on the packaging label.
The products were shipped to distributors and further processors in New York and Pennsylvania.
The problem was discovered when FSIS collected a routine product sample that confirmed positive for the presence of E. coli O157:H7. There have been no confirmed reports of adverse reactions due to consumption of these products.
Anyone concerned about an illness should contact a healthcare provider. E. coli O157:H7 is a potentially deadly bacterium that can cause dehydration, bloody diarrhea and abdominal cramps 2–8 days (3–4 days, on average) after exposure the organism. While most people recover within a week, some develop a type of kidney failure called hemolytic uremic syndrome (HUS). This condition can occur among persons of any age but is most common in children under 5-years old and older adults. It is marked by easy bruising, pallor, and decreased urine output. Persons who experience these symptoms should seek emergency medical care immediately.
FSIS is concerned that some product may be frozen and in cold storage at distributor or further processor locations. Distributors and further processors who received these products are urged not to utilize them.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume whole cuts of beef that have been cooked to a temperature of 145 °F with a 3-minute rest time and ground beef to 160 °F. The only way to confirm that beef is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, https://www.fsis.usda.gov/safetempchart.
Consumers with questions about the recall can contact Mr. Kim Holzner, Head of JBS Imports, at Kim.Holzner@jbssa.com. Members of the media with questions about the recall can contact Ms. Nikki Richardson, Director of Communications for JBS USA Food Company, at Nikki.Richardson@jbssa.com.

Olymel S.E.C./L.P. Recalls Ready-to-Eat Ham Products Due to Possible Salmonella Enteritidis Contamination

April 15, 2021

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WASHINGTON, APRIL 15, 2021 – Olymel S.E.C./L.P., a Quebec, Canada establishment, is recalling approximately 6,804 pounds of ready-to-eat (RTE) ham products that may be contaminated with Salmonella Enteritidis, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The ham items were packaged on November 5, 2020. The following products are subject to recall [View Labels (PDF Only)]:
•    12-lb. plastic film vacuum package of “Celebrity EXTRA LEAN IMPORTED HAM 98% FAT FREE” with product codes “20309 11 – 91”, “20309 21 – 91”, “20309 31 – 91” or “20309 51 – 91” printed on the side of the packaging.
The products subject to recall bear Canadian establishment number 180 inside the Canadian inspection mark located below the ingredient list. These items were shipped to distributors in California for further distribution for institutional use.
The problem was discovered when FSIS collected a routine product import sample that confirmed positive for the presence of Salmonella Enteritidis¬¬¬. The product subject to recall was determined by the Canadian Food Inspection Agency (CFIA) to be associated with the FSIS positive sample result.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider. 
Consumption of food contaminated with Salmonella can cause salmonellosis, one of the most common bacterial foodborne illnesses. The most common symptoms of salmonellosis are diarrhea, abdominal cramps, and fever within 6 hours to 6 days after eating the contaminated product. The illness usually lasts 4 to 7 days. Most people recover without treatment. In some persons, however, the diarrhea may be so severe that the patient needs to be hospitalized. Older adults, infants, and persons with weakened immune systems are more likely to develop a severe illness. Individuals concerned about an illness should contact their health care provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Media and consumers with questions regarding the recall can contact Richard Vigneault, Media Relations for Olymel S.E.C./L.P., at (514) 497-1385 or rvigneau@videotron.ca. Members of the media can also contact Lennert Berg, COO for Atalanta Corp., at (908) 372-6064. Consumers with questions can also contact Glenn Gaus, Director of Food Safety & Quality Assurance for Atalanta Corp., at (908) 845-2079.

Torn & Glasser Recalls Dark Chocolate Espresso Beans Because of Undeclared Walnut Allergen

April 13, 2021

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Torn & Glasser of Los Angeles, CA is recalling 7464 units of dark chocolate espresso beans due to an undeclared allergen. The dark chocolate walnuts were mislabeled as “dark chocolate espresso beans”. People who have an allergy or severe sensitivity to walnuts run the risk of serious or life-threatening allergic reaction if they consume this product.
No illnesses have been reported to date.
The mislabeled dark chocolate espresso beans were sold at Kroger divisions in the following 30 states under the banners (Kroger, Arlan’s, Fred Meyer, Smiths, Food For Less. Fry’s Food Stores, Ralphs, Dillons, Roundy’s Chicago, Roundy’s Mariano’s) beginning March 3rd, 2021.
Alaska, Alabama, Arizona, Arkansas, California, Georgia, Illinois, Indiana, Idaho, Kansas, Kentucky, Louisiana, Michigan, Mississippi, Missouri, Montana, Nebraska, Nevada, New Mexico, Ohio, Oregon, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, Wyoming
Product affected by this recall is listed below.
UPC#    Description    LOT#    Expiration Date
0 72488 99868 1    Torn & Glasser Dark Chocolate Espresso Beans with green leaf logo on top 12 OZ TUBS    777739    Best if used by: 11/19/2021
The recall was initiated after it was discovered that product containing walnuts was packaged in a container that the top label listed Dark Chocolate Espresso Beans and the bottom label listed Dark Chocolate Walnuts. Subsequent investigation indicates that the wrong label was used by Production personnel.
Customers who purchased the above list of products with associated lot are urged to destroy the product and/or return it to the place of purchase for a full refund. Consumers with questions may contact the company at (213) 627-6496 Monday – Friday 7:00AM – 4:00PM or 1622 East Olympic Boulevard, Los Angeles, California, 90021

Voluntary Recall of Hostess® SnoBalls® Due to Undeclared Allergen

April 10, 2021

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Hostess Brands, LLC (”Hostess Brands“) has become aware that certain Hostess® SnoBalls® were inadvertently manufactured in the packaging for Hostess® Chocolate CupCakes and the packaging does not list ”coconut“, an ingredient in SnoBalls®, as an allergen. Hostess Brands is voluntarily recalling the following SnoBalls® manufactured on March 13, 2021:
Product    Item UPC    Batch    Best By Date
Hostess® SnoBalls® (single-serve)    888109010096    I031221000    May 27, 2021
The products were sold to convenience stores, dollar stores, and distributors throughout the United States. No injuries or illnesses have been reported to date. Consumers who have purchased the affected product are urged to discontinue consumption and contact the place of purchase about returning them for a full refund.
No other varieties of Hostess® SnoBalls® are affected.
Consumers with questions may contact 1-800-483-7253 and also visit www.hostesscakes.comExternal Link Disclaimer.

FSIS Issues Public Health Alert for Raw Ground Turkey Products Linked to Salmonella Hadar Illness

April 10, 2021

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WASHINGTON, APRIL 10, 2021 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for approximately 211,406 pounds of raw ground turkey products, produced by Plainville Brands, LLC, a Pennsylvania establishment, due to concerns the products may have caused Salmonella Hadar illness. A recall was not requested because it is believed that the products are no longer available for consumers to purchase.
 FSIS is concerned that some product may be frozen and in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. Retail locations that may receive returned product from consumers should destroy this product immediately.
The raw ground turkey products were produced on December 18, 2020 through December 29, 2020. The following products are subject to the public health alert:
•    1-lb. packages of Nature’s Promise Free from 94% LEAN | 6% FAT Ground Turkey with Use by/freeze/sell by date of 1/1/21, 1/3/21,1/4/21, 1/8/21 and 1/10/21 on the front of the package.
•    1-lb. packages of Wegman 94% LEAN | 6% FAT Ground Turkey with Use by/freeze/sell by date of 1/3/21, 1/4/21, 1/8/21 and 1/10/21 on the front of the package.
•    3-lb. packages of Wegman 94% LEAN | 6% FAT Ground Turkey with Use by/freeze/sell by date of 1/3/21, 1/4/21, 1/8/21 and 1/10/21 on the front of the package.
•    1-lb. packages of Plainville Farms Ground White Turkey 93% | 7% Fat with Use by/freeze/sell by date of 1/10/21 on the front of the package.
The products bear establishment number EST. P-244 inside the USDA mark of inspection. These items were shipped to retail locations nationwide.
FSIS and its public health partners, including the Centers for Disease Control and Prevention (CDC), public health and regulatory officials are investigating a multistate outbreak of 28 Salmonella Hadar illnesses in 12 states with onset dates ranging from December 28, 2020 through March 4, 2021. The traceback investigation for one case patient identified the patient consumed ground turkey produced by Plainville Brands, LLC. An intact, unopened package of Plainville Brands’ ground turkey collected from this case-patient’s home tested positive for Salmonella Hadar and was closely related genetically to the sample from the patient. Evidence collected to date does not link all illnesses to this establishment. Based on the continuing investigation, additional product from other establishments may be involved. FSIS continues to work with CDC and state and local public health partners on this investigation and will provide updated information as it becomes available.
Consumption of food contaminated with Salmonella can cause salmonellosis, one of the most common bacterial foodborne illnesses. The most common symptoms of salmonellosis are diarrhea, abdominal cramps, and fever within 12 to 72 hours after eating the contaminated product. The illness usually lasts 4 to 7 days. Most people recover without treatment. In some persons, however, the diarrhea may be so severe that the patient needs to be hospitalized. Older adults, infants, and persons with weakened immune systems are more likely to develop a severe illness. Individuals concerned about an illness should contact their health care provider.
FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume raw ground turkey that has been cooked to a temperature of 165°F. The only way to confirm the poultry item is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, https://www.fsis.usda.gov/safetempchart.
Consumers and members of the media with questions about the public health alert can contact Yusef Robb at (323)384-1789 or by email at yusef@tkCommunicationsLLC.com.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.
https://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-raw-ground-turkey-products-linked-salmonella-hadar

Glutenull Bakery Issues Allergy Alert on Undeclared Milk in Goji Berries and Chocolate Cookies

April 7, 2021

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Glutenull Bakery of Port Coquitlam, BC, Canada is recalling Goji Berries and Chocolate Cookies 11oz/320g, because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of allergic reaction if they consume this product.
Product was distributed in WA and OR in retail stores such as Whole Foods Market and Market of Choice.
The Glutenull Goji Berries and Chocolate Cookies product is packaged in clear plastic clamshell container with paper sleeve, net wt. 11 oz / 320g, and has the UPC 628451529132. The recalled product has all lots with the expiration dates 06/10/2021 to and including EXP 08/20/2021. No illnesses have been reported to date, no customer complaints.
The recall was initiated after it was discovered that vegan chocolate used in the product Goji Berries and Chocolate Cookies had traces of milk proteins which occurred due to cross contamination at the chocolate supplier’s facility. The Goji Berries and Chocolate Cookies were distributed in packaging that did not include “may contain milk” statement.
This recall is being made with the knowledge of the U.S. Food and Drug Administration.
Consumers who have purchased Goji Berries and Chocolate Cookies are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at info@glutenull.com by email or call us directly at +1(604) 777-5596, Monday – Friday, 9 am – 4 pm PST.
Now Glutenull Bakery is making their own in house made chocolate (vegan, gluten free, non-GMO, HAACP certified) to eliminate any possible risk of cross contamination of milk. The new chocolate is now being used in Glutenull Goji Berries and Chocolate Cookies and distributed to stores. See link for the chocolate production below: https://youtu.be/ZjgGimzKyK8

FSIS Issues Public Health Alert for Raw Ground Chorizo Sausage Products Due to Possible Foreign Matter Contamination

April 5, 2021

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EDITOR’S NOTE: FSIS updated the release the same day of issue to reflect product poundage.
WASHINGTON, April 2, 2021 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for for approximately 39 pounds of raw ground chorizo sausage products due to concerns that the products may be contaminated with extraneous materials, specifically hard pieces of crystalline material. FSIS is issuing this public health alert out of the utmost of caution to ensure that consumers are aware that these products should not be consumed. A recall was not requested because it is believed that the products are no longer available for consumers to purchase.
The fresh and frozen raw ground chorizo sausage items were produced on March 8, 2021 by Century Oak Packing Company, an establishment in Mt. Angel, Ore. The following product is subject to the public health alert:
•    1-lb. packages containing “Lonely Lane Farms Family Farm Since 1939 OREGON RAISED Chorizo Sausage” and product ID 21067-6.
The products bear establishment number “EST. M40256” inside the USDA mark of inspection. These items were sold at a farmer’s market and also shipped to retail locations in Oregon.                                 
The problem was discovered when the firm received three consumer complaints reporting findings of hard pieces of crystalline material in the product.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
FSIS is concerned that some product may be in consumers’ refrigerators or freezers or both. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers with questions can contact Century Oak Packing at 503-845-4180. Members of the media with questions about the public health alert can contact Evelyn Shop, Media and Communications Director at Century Oak Packing at (718) 772-2350.

Rong Shing Trading Inc. Recalls Ineligible Beef Products Imported from China

April 2, 2021

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WASHINGTON, April 1, 2021, Rong Shing Trading Inc., a Brooklyn, N.Y. firm, doing business as Double R Trading Inc., is recalling approximately 3,365 pounds of Chinese style hot pot base products containing beef tallow. The products were imported from the People’s Republic of China, a country ineligible to export beef to the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The Chinese style hot pot base products were imported on or around February 14, 2020. The following products are subject to recall:
•    450g Plastic vacuum wrapped packages containing a “Lee’s 52° Da Zhuang” Hot Pot Base and a Sell By date of January 29, 2022 on the label.
 
•    300g Plastic vacuum wrapped packages containing a “Lee’s 45° Da Zhuang” Hot Pot Base and a Sell By date of June 30, 2021 on the label.
The product labels are written in the Chinese language. Refer to the label link here for additional product information. The products do not bear an establishment number nor a USDA mark of inspection. These items were shipped to retail locations nationwide.                            
The issue was identified after FSIS received a consumer complaint.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.  
FSIS is concerned that some product may be in consumers’ homes. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

Harris Teeter Announces Voluntary Recall of Fresh Foods Market Cookies & Crème Cakes Due to Undeclared Hazelnut

March 31, 2021

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Harris Teeter announced today the voluntary recall of Fresh Foods Market items due to undeclared hazelnut.
The items included in the recall are:
Harris Teeter Fresh Foods Market 8-inch Three-Layer Cookies & Creme Cake UPC: 0007203695224
Harris Teeter Fresh Foods Market Cookies & Creme Cake Halves UPC: 0007203695846
Harris Teeter Fresh Foods Market Cookies & Creme Cake Slices UPC: 0007203695862
Upon notification of this recall by its supplier, Rise Baking Company, Harris Teeter promptly removed the product from its shelves.
Shoppers who purchased one or more of these items and have an allergy or sensitivity to hazelnut should not consume them. Instead, they should return items to Harris Teeter for a full refund.
Harris Teeter is using transactional data to identify shoppers who may have purchased the product as well as listing complete information on the homepage of harristeeter.com.
Of the nearly 29,000 transactions which occurred within the recall timeframe, Harris Teeter has initiated contact with 27,317 shoppers by phone and/or email using loyalty card data to inform them of the recall.

Sabra Dipping Company Issues Limited Voluntary Recall of a Single SKU of Classic Hummus

March 31, 2021

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Sabra Dipping Company, LLC announced that, in partnership with the FDA, it is voluntarily recalling approximately 2,100 cases of 10 oz Classic Hummus because it was potentially contaminated with Salmonella, that was discovered by a routine screen of a single tub by the FDA. The recall is limited to 1 SKU of 10 oz Classic Hummus produced on Friday, February 10, 2021 between the hours of 6:00 PM and 12:00 midnight with a “Best Before” date of April 26.
The voluntary recall is limited only to 10 oz Classic Hummus. No other Sabra products are affected by this recall. This product was distributed to 16 states. The product is over halfway through its shelf life. It’s unlikely you’ll find this product on the shelf. No illnesses or consumer complaints have been reported to date in connection with this recall.
The recalled product is listed below. Consumers can find time stamp and “Best Before” date on the top of each package.
UPC    Item    Best Before    PRODUCTION DATE/TIME STAMP
300067    Classic Hummus, 10oz    4/26/21    On: Feb 10
Between: 18:00:27 and 23:49:00
The product was distributed in the following states: Alabama, Arizona, Arkansas, California, Florida, Indiana, Mississippi, Maine, Missouri, Nebraska, North Carolina, New Jersey, Utah, Virginia, Washington and Wisconsin.
Consumers can contact Sabra Consumer Relations at 1-866-265-6761 for additional information Monday – Friday from 8 AM to 8 PM Eastern Standard Time. Additionally, consumers who have purchased the specific recalled product are urged to return it to the place of purchase or visit www.sabrahummusrecall.comExternal Link Disclaimer for product reimbursement.

EXPANDED RECALL: Avanza Pasta, LLC Recalls Beef and Poultry Products Produced Without Benefit of Inspection

March 31, 2021

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Editor’s note: This recall was updated on March 29, 2021 to reflect changes to the products included in the recall. Additional products and labels have been added to the linked documents.
WASHINGTON, March 20, 2021 – Avanza Pasta, LLC., an Evanston, Ill. establishment, is recalling approximately 9,847 pounds of meat and poultry pasta products that were produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The meat and poultry ravioli and tortellini items were produced on various dates from October 5, 2019 through March 12, 2021. The products subject to recall can be found here:
The products subject to recall do not bear an establishment number nor the USDA mark of inspection. These items were shipped to restaurants, distributors, and retail locations in Illinois, Indiana and Wisconsin.                         
The problem was discovered by FSIS during in-commerce surveillance activities.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.  
FSIS is concerned that some product may be frozen and in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Pavlos Loumbroukos, Operations Manager for Avanza Pasta, LLC., at (847) 584-2891.

Trident Seafoods Recalling Pacific Salmon Burger

March 27, 2021

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Trident Seafoods Corporation is issuing a voluntary recall of a single lot number of Pacific Salmon Burgers, Net Wt. 3 lbs. (48 oz.), because it may contain small pieces of metal. Consumption of these products may pose a choking hazard or other physical injury. If you have any remaining product with Lot Number GC101431 and a Best By 01/14/2023, please discontinue use and return item to your local Costco for a full refund.
There have been no reports of injury or illness related to the recalled products to date, however anyone concern about an injury or illness should contact a healthcare provider. The source of the small pieces of metal hasn’t been identified yet. Trident Seafoods takes food safety very seriously and is investigating this situation thoroughly.
For additional information, please contact our Consumer Affairs Team, at 1-866-413-4749, Monday – Friday, 8 a.m. – 5 p.m. PST, or via email to consumeraffairs@tridentseafoods.com.  We apologize for any inconvenience this may have caused.

Trident Seafoods Recalling Pacific Salmon Burger

March 27, 2021

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Trident Seafoods Corporation is issuing a voluntary recall of a single lot number of Pacific Salmon Burgers, Net Wt. 3 lbs. (48 oz.), because it may contain small pieces of metal. Consumption of these products may pose a choking hazard or other physical injury. If you have any remaining product with Lot Number GC101431 and a Best By 01/14/2023, please discontinue use and return item to your local Costco for a full refund.
There have been no reports of injury or illness related to the recalled products to date, however anyone concern about an injury or illness should contact a healthcare provider. The source of the small pieces of metal hasn’t been identified yet. Trident Seafoods takes food safety very seriously and is investigating this situation thoroughly.
For additional information, please contact our Consumer Affairs Team, at 1-866-413-4749, Monday – Friday, 8 a.m. – 5 p.m. PST, or via email to consumeraffairs@tridentseafoods.com.  We apologize for any inconvenience this may have caused.

Kareem Mart Recalls “Halva” Because of Possible Health Risk

March 26, 2021

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Kareem Mart of Garden City, MI,is recalling its 1lb and 2lb Kareem Chef brand “Halva”, “Halva with Pistachio”, and “Halva with Chocolate” food treats because they have the potential to be contaminated with salmonella, an organism which can cause serious and sometimes fatal infection in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, producing more severe illnesses infections.
The recalled “Halva” were distributed through Mediterranean food stores and wholesalers in Michigan, Illinois, Missouri, New York, Ohio, North Carolina and Pennsylvania.  Between March 2020 to Feb 2021.
Please do not consume the product and immediately dispose of the product or return to 32816 Manor Park Garden City MI 48135. Or to the place of purchase. And send us a note to the email: recalls@kareemmart.com with the return receipt and product purchase date for a full refund.
The products come in 1lb and 2lb plastic tubs. There is only one lot distributed.
With Best Before 07-01-2022.
No illnesses have been reported to date in connection with the problem.
The potential for contamination was noted after routine testing from samples in the stores by the Michigan Department of Agriculture and Rural Development (MDARD).
Production of the product has been suspended while the FDA and the company continue their investigation as to the source of the problem.

Durisan Hand Sanitizer Recall Due to Microbial Contamination

March 25, 2021

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Sanit Technologies LLC d/b/a Durisan announces a voluntary recall of the lots listed in the table below of Durisan Antimicrobial Hand Sanitizer, Non-Alcohol products in various sizes listed. The products are being recalled due to microbial contamination. Specifically, out of specification results for bacterial count for Burkholderia cepacia complex and Ralstonia pickettii. The issue was discovered during a routine audit focused on production scale-up during the height of the pandemic.
Durisan Antimicrobial Solutions Hand Sanitizer Sizes With the Following Identification
Volume mL    Volume oz.    UPC    NDC
18    0.61    8 52379 00614 1    71120-112-01
118    4    8 52379 00634 9    71120-112-10
236    8    8 52379 00635 6    71120-112-11
300    10    8 52379 00697 4    71120-112-08
550    18.59    8 52379 00620 2    71120-112-06
1000    33.81    8 52379 00610 3    71120-112-05

Lot Numbers
DHS030920A1-A    DHS051420A1-S
DHS030920A2-S    DHS051420A1-S
DHS030920A3-S    DHS052020B1-S
DHS031020A4-S    DHS052020C1-S
DHS031020A5-3    DHS052220B1-S
DHS031020A6-S    DHS052620B1-S
DHS031020A7-S    DHS052720C1-S
DHS031020A8-S    DHS052720D1-S
DHS031120A1-S    DHS052820B1-S
DHS031120A2-S    DHS052820C1-S
DHS031120A3-S    DHS052820D1-S
DHS031120A4-S    DHS060120A1-S
DHS031120A5-S    DHS060220A1-S
To date, no reports of adverse reactions or customer complaints have been reported related to this recall.
The product was packaged in sizes ranging from 18mL credit cards, to bottles sized in 118, 236, 300 and 550 mL and 1000mL wall mounted dispenser refills. Pictures are available in the attached related file.
Use of a hand sanitizer contaminated with Burkholderia cepacia complex and Ralstonia pickettii, can range from no reaction to serious infections in a person with a hand wound or scrapes because the bacteria could enter the bloodstream, especially in patients with compromised immune systems. Health care professionals who use this contaminated hand sanitizer and tend to an at-risk patient, such as one with cystic fibrosis, could lead to adverse events ranging from a localized infection to lung or bloodstream infections, which could require patient hospitalization.
The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available. The product can be identified by examples of the product labels below. The product was manufactured from Feb. 1, 2020 until June 30, 2020, and distributed to selected retailers nationwide in the United States.
Durisan has provided written notification to its distributors and retailers and is alerting customers via this voluntary recall. Consumers that have the product which is being recalled are advised to destroy it immediately.
Consumers with questions regarding this recall can contact Durisan at 941-351-9114, 8:30 am - 4:30 pm Eastern time, Monday through Friday or by e-mail at customerservice@durisan.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug.

GK Foods USA Announces Voluntary Recall of a Batch of La Fe Peppers and Onions

March 25, 2021

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GraceKennedy Foods (USA) LLC (GK Foods USA) has announced a voluntary recall of a batch of its La Fe Peppers and Onions, due to the probable presence of extraneous material.
Derrick Reckord, President and CEO of GK Foods USA, owner of the La Fe brand, explained that the Voluntary Class 2 Recall has been initiated because there possibly could be small pieces of blue plastic in the product. If consumed, these plastic pieces could cause adverse health consequences. A Class 2 recall is issued when there is a remote probability of adverse health effects from the consumption of a product.
Mr. Reckord went on to say that there have been no reports of any adverse health issues associated with the affected product to date, and that GK Foods USA was recalling the entire batch out of an abundance of caution.
The batch of La Fe Peppers and Onions being recalled by Grace Foods USA comprises of 187 cases of the product which has been distributed in the North-East USA only. The product is included in La Fe’s vegetable blends category, and more details on the batch being recalled can be found below:
•    Brand/Product – La Fe Peppers & Onions
•    Net Weight – 16oz
•    Batch Number – Lot # KR043021
•    Best Before Date: March 2023
The best before dates and batch number can be found on the back panel of the packaging, close to the universal product code (UPC) bar code.
Consumers who purchased La Fe Peppers and Onions bearing the above best before dates and corresponding batch number, should not consume them. Instead, they should return the product to the point of purchase, where they will be refunded in full for the item(s) purchased.
“GK Foods USA wishes to assure consumers that their safety is always considered paramount. Providing safe, high quality products remains our number one priority,” Mr Reckord said. He also emphasized that the voluntary recall does not include any other batches of La Fe Peppers and Onions or any other La Fe products.
Consumers with questions pertaining to the recall may contact Ricardo Bryan at GK USA at 201.329.6260 ext. 5137 Mondays to Fridays between the hours of 9 a.m. and 5 p.m. EST. or via email to ricardo.bryan@gkco.com.

Real Water, Inc., Issues Precautionary Recall of All Sizes of Real Water Brand Drinking Water Due to a Possible Health Risk

March 25, 2021

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Real Water, Inc. of Mesa, AZ and Henderson, NV, has issued a voluntary recall of all sizes of its Real Water brand drinking water, because it may be linked to certain instances of non-viral hepatitis which were reported in or about November, 2020 in the Las Vegas, NV area. 
Symptoms of all types of hepatitis, including non-viral hepatitis, are similar and can include fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, dark urine, clay or gray-colored bowel movements, joint pain, yellow eyes, and jaundice. Those experiencing these symptoms should contact their doctor.
Recalled products include 1.5 liters, 1 liter, 500 ml and 1 gallon ready-to-drink bottles that were distributed throughout the United States by UNFI and KEHE to the natural channel of stores, as well as through direct distribution to various retail stores on a regional basis in the greater Las Vegas, NV area, Northern Arizona, Southern California, Tennessee, Georgia, Chicago, New York, Mississippi, and New Mexico.  Real Water is also sold on Amazon.com.  In addition, 5-gallon home and office delivery bottles were distributed through direct delivery to homes and offices in the greater Las Vegas, NV area, central California coastal region (North of Los Angeles, CA and South from Santa Barbara, CA), and Phoenix, AZ.  Also included in the recall are the 4 oz bottles of Real Water Concentrate, sold on the Firm’s website.
The ready-to-drink bottles sold in retail stores have a blue rectangular bottle with “Real Alkalized Water” printed on the label. 5-Gallon home and office delivery bottles are blue with white labels.
Distributors have been notified of the recall and instructed to immediately remove recalled products from all store shelves, distribution, and other inventories to ensure they are no longer available for sale or consumption. Home and office delivery customers have also been instructed how to have products picked up.
The recall is the result of an investigation by the Southern Nevada Health District and the FDA after reported cases of non-viral hepatitis in or about November 2020 were suspected to be potentially linked to Real Water’s 5-gallon Home and Office Delivery.  Real Water takes customer safety seriously and promptly issued this recall on March 17, 2021 after being notified of the investigation.  The company has ceased production and distribution of the product as the FDA and the company continue their investigations into the potential cause of the problem.
Consumers who may have recalled products should discard it immediately and not drink it.  Customers of Real Water’s 5-gallon Home and Office Delivery should contact Real Water at the number or email below to have any remaining product picked up. Consumers who have purchased Real Water ready-to-drink bottles may return it to the place of purchase for refund. Consumers with questions, or to obtain a refund, may contact the company at 1-702-310-5437 on Monday through Saturday from 8 a.m. to 5 p.m. Pacific time or by email at customerservice@drinkrealwater.com.

BC Food LA, LLC Recalls Ineligible Beef Products Imported From China

March 25, 2021

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BC Food LA, LLC., a South El Monte, Calif. firm, doing business as B & C Food Co., is recalling approximately 1,643 pounds of Chinese style hot pot base products containing beef tallow. The products were imported from the People’s Republic of China, a country ineligible to export beef to the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The Chinese style hot pot base products were imported on or around June 24, 2020. The following products are subject to recall: [View Labels (PDF Only)]:
•    10.5-oz. (300 g) Plastic vacuum wrapped packages containing a “Lee’s 52° Da Zhuang” Hot Pot Base and a best before date of 10/12/2021 on the label.
•    10.5-oz. (300 g) Plastic vacuum wrapped packages containing a “Lee’s 45° Da Zhuang” Hot Pot Base and a best before date of 10/12/2021 on the label.
•    10.5-oz. (300 g) Plastic vacuum wrapped packages containing a “Lee’s 36° Da Zhuang” Hot Pot Base and a best before date of 10/12/2021 on the label.
The product labels are written in the Chinese language. Refer to the label link here for additional product information. The products do not bear an establishment number nor a USDA mark of inspection. These items were shipped to retail locations in California, Nevada, and Oklahoma.
The problem was discovered when FSIS received an anonymous report of ineligible beef tallow products imported from China.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.  
FSIS is concerned that some product may be in consumers’ homes. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls

Hannaford Brothers Recalls Select Taste of Inspirations Wing Sauce Lots Recalled Due to Undeclared Allergen

March 25, 2021

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Hannaford Supermarkets is recalling select lots of Taste of Inspirations Parmesan Wing Sauce because the contents of the bottle do not match the label. The bottles were incorrectly filled with Taste of Inspirations Garlic Parmesan Dressing and have an undeclared allergen, fish. Impacted products include the following information on the bottle:
•    Lot code 210305 and a Best By Date of March 5, 2022
Customers with fish allergies who purchased the impacted products should not consume them. All customers who purchased the product may return the item to a Hannaford store for a full refund.
No injuries or illnesses have been reported.

Bobo’s Issues a Voluntarily Allergy Alert on Undeclared Peanuts in Product

March 23, 2021

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Bobo’s of Boulder, Colorado is issuing a voluntary recall of Bobo’s Maple Pecan Oat Bars because they may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Maple Pecan Bars were distributed through retail stores nationwide and through online orders at www.eatbobos.com.
The product can be identified by the lot code found on a stamp on the back of the bar: 0L30112B, Best By 7/30/21 or 7/31/21. The bars are 3oz and may be a single bar or in a box of 12. UPC Code: 829262000210
No illnesses have been reported to date.
The recall was initiated after it was discovered that product containing peanuts was distributed in packaging that did not reveal the presence of peanuts on the ingredient deck.
No other Bobo’s product with this best buy date was impacted.
Consumers who have purchased the affected lot should return the product to where it was purchased to request an exchange or full refund if there is an allergy concern. Affected product should then be discarded in a secure place and not consumed.
For more information, please contact us at info@eatbobos.com or 303-938-1977 between Monday – Friday, 8am-4pm MDT.

Food Lion Recalls Select Taste of Inspirations Parmesan Garlic Wing Sauce

March 22, 2021

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Food Lion is recalling select lots of Taste of Inspirations Parmesan Garlic Wing Sause because they were mislabeled and contain an undeclared allergen (fish). The impacted products may have been purchased between Feb. 20, 2021 – March 20, 2021, and include the following information on the bottle:
•    Lot code 210305 and a Best By Date of March 5, 2022
Customers with fish allergies who purchased the impacted products should not consume them. All customers who purchased impacted product may return it to their local Food Lion store for a refund equal to double the purchase price in accordance with Food Lion’s “Double Your Money Back Guarantee."

Three Turkey Wrap Sandwiches Added to Mg Foods’ Previous Recall List Due to Possible Listeria Monocytogenes Contamination

March 20, 2021

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MG Foods of Charlotte, NC is expanding its recall issued March 10, 2021 to include three Turkey Wraps due to potential contamination of Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short- term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, a Listeria monocytogenes infection can cause miscarriages and stillbirths among pregnant women.
The products were distributed between March 3, 2021 and March 5,  2021 and packaged in clear plastic wedges & plastic wrap. The products were sold exclusively via vending machines and micro markets located in business locations in Georgia, North Carolina, South Carolina, and West Virginia. The company reacted swiftly and as of end-of-day March 5, 2021 affected products were removed from sale at all locations.
No illnesses have been reported to date.
PRODUCT    SIZE    UPC    CONTAINER    USE BY DATES
Fresh to You Deluxe Club Wrap    10.39 oz    MGF9814    Plastic Wedge    3/7/2021
MG Foods Roasted Turkey in a Tomato Basil Wrap    6.90 oz    1 00000 50005 7    Plastic Wedge    3/7/2021
MG Foods The Club in a Spinach Wrap    8.50 oz    1 00000 50008 8    Plastic Wedge    3/7/2021
Product labels are attached for identification of products.
Consumers who have purchased these products are urged to discard any remaining product. Consumers may contact MG Foods at 1-855-424-8390 Monday thru Friday 7:00am – 7:00 pm EST for any questions related to this recall or to request a full refund.

Avanza Pasta, LLC Recalls Beef and Poultry Products Produced Without Benefit of Inspection

March 20, 2021

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Avanza Pasta, LLC., an Evanston, Ill. establishment, is recalling approximately 2,237 pounds of meat and poultry pasta products that were produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The meat and poultry ravioli and tortellini items were produced on various dates from October 5, 2019 through March 12, 2021. The products subject to recall can be found here:
The products subject to recall do not bear an establishment number nor the USDA mark of inspection. These items were shipped to restaurants, distributors, and retail locations in Illinois, Indiana and Wisconsin.                         
The problem was discovered by FSIS during in-commerce surveillance activities.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.  
FSIS is concerned that some product may be frozen and in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Pavlos Loumbroukos, Operations Manager for Avanza Pasta, LLC., at (847) 584-2891.

FSIS Issues Public Health Alert for Beef and Lamb Products Produced Without Benefit of Inspection

March 19, 2021

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The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for products produced without the benefit of federal inspection by One Meat Corp., doing business as Eastern Asia Trading Corporation, a La Puente, Calif. firm. A recall was not recommended because it is believed that the affected products are no longer available to be purchased by consumers.
The beef and lamb products subject to the public health alert are:
•    1-lb packages of Eastern Asia Trading Corporation “BEEF OMASUM TRIPES.”
 
•    1-lb packages of Eastern Asia Trading Corporation “GROUND LAMB” with “Production date” 12/26/2020.
 
•    1-lb packages of Eastern Asia Trading Corporation “CUTTED BEEF FOR BBQ” with “Production date” 7/31/2020.
 
•    1-lb packages of Eastern Asia Trading Corporation “CHINESE LAMB BBQ.”
 
•    2-lb packages of Eastern Asia Trading Corporation “CUTED BEEF LIGAMENT.”
 
•    Approx. 1-lb packages of Eastern Asia Trading Corporation “CHINESE BEEF BBQ.”
 
•    1-lb packages of Eastern Asia Trading Corporation “CUBED LAMB FOR BBQ SET.”
While some products bear the establishment number “EST. 45557” inside the USDA mark of inspection, the products were not produced by federal establishment 45557.
 The items were shipped to an online retailer, Weee! Corporation, and sold directly to consumers through online sales nationwide.
FSIS is concerned that some product may be in consumers’ freezers. Anyone concerned about an illness should contact a health care provider. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and media with questions regarding the public health alert should call Bruce Park, President of One Meat Corp., at (213) 238-7863.

Mindo Chocolate Makers Issues Allergy Alert on Undeclared Milk in “Coffee Toffee Chocolate Bar

March 18, 2021

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MINDO CHOCOLATE MAKERS OF Dexter, Michigan, is recalling its Coffee Toffee Chocolate Bar (75 grams/2.65oz) because of the undeclared presence of milk, a major allergen, in the butter used to make the toffee in the bar. People with milk allergies are at risk of potentially serious or life-threatening reactions if they consume this product.
The recalled Coffee Toffee Chocolate Bars were distributed primarily in the state of Michigan in retail stores and through online orders.
The product comes as a 75 gram/2.65oz bar in a white paper wrapper labeled with Lot Numbers 190310 through 210310.
No illnesses have been reported to date in connection with this problem.
The recall was initiated after it was discovered that the mislabeled product was distributed in packaging that did not reveal the presence of milk. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's packaging processes.
Distribution of the affected products has been suspended until the FDA and the company are certain that the problem has been corrected.
Consumers who have purchased Coffee Toffee Bars (75 grams/2.65oz) that have labels that do not say “contains milk” or do not have milk stated in the ingredients are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-734-660-5635 Monday to Friday 8AM to 5PM.

Western Mixers Produce & Nuts, Inc. Recalls Gelson’s Yogurt Raisins Because of Possible Allergen Heath Risk

March 18, 2021

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Western Mixers Produce & Nut Company of Los Angeles, California is recalling the following item:
Gelson’s Yogurt Raisins, 14 oz. because it may contain undeclared Peanuts. People who have an allergy or severe sensitivity to Peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Gelson’s Yogurt Raisins were distributed in: California; through Retail Stores, during the dates of: February 4, 2021 – March 11, 2021.
No illnesses have been reported to date.
The recall was initiated after it was discovered that product containing Peanuts was distributed in packaging that did not reveal the presence of Peanuts. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company’s production and packaging processes.
The company has corrected the Nutritional Panel and Ingredient Statement on their labels for the production and distribution of the product as FDA, ARO and Western Mixers continue with their investigations.
Consumers who have purchased Gelson’s Yogurt Raisins 14 oz., with reference to the above Lot numbers, are urged to destroy the product and/or return it to the place of purchase for a full refund. Consumers with questions may contact Western Mixers Produce & Nuts, Inc. at: 1-877-230-8449, Monday through Friday, between the hours of 7:00 am (PST) and 2:00 pm (PST).
The Gelson’s Yogurt Peanuts can be identified as follows:
Package Size    Package Label    Product Detail    Lot # On Pkg.
14 oz. Clear Plastic Clamshell    Gelson’s
Retailer: Gelson’s    Yogurt Raisins 14 oz.    #210330
Sell By Date: 02/02/22

PNHC, LLC d/b/a Heal the World Issues Voluntary Nationwide Recall of Heal the World Hand Sanitizer Packaged in 9.6 Ounce Bottles Because They Resemble Small Water Bottles

March 17, 2021

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Raleigh, North Carolina, PNHC, LLC, d/b/a Heal the World, is voluntarily recalling all lots of Heal the World hand sanitizer packaged in 9.6 fl. oz containers to the consumer level. The products are being recalled because they resemble 9.6ounce water bottles. The recall does not affect any other Hand Sanitizer products from PNHC, LLC and/or Heal the World.
Product    Size    NDC
Heal the World Hand Sanitizer    9.6 FL. OZ (285 mL)    73333-285-01
Lot Nos. SAA21, SAA24, SAA27, SAA22, SAA23, SAA29, SAA26, SAA28, SAA25, SAA32, SAA55, SAA56, SAA44, SAA60.
Ingesting hand sanitizer, which is intended for topical use, could potentially result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal. Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute.  To date, PNHC, LLC, d/b/a Heal the World has received no reports of adverse reactions and no complaints have been received.
The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available and is packaged in 9.6 ounce plastic bottles. The product can be identified by the bottle’s label pictured below. Product was distributed to selected retailers in the United States.
PNHC, LLC has provided notification to its distributors and retailers. Distributors and retailers that have product which is being recalled should stop distribution. While the product is not available for purchase and has not been available for several months, if a consumer has product which is being recalled he or she is advised to contact the entity who sold the product to consumer for return.
Consumers with questions regarding this recall can contact PNHC, LLC at 813-434-0741 from 9:00 am- 5:00 pm EST, Monday through Friday. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online by regular mail or by fax.
•    Complete and submit the report OnlineExternal Link Disclaimer
•    Regular Mail or Fax: Download formExternal Link Disclaimer or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Allergy Alert Issued for Undeclared Tree Nuts in Mislabeled Cranberry Biscotti at Six Whole Foods Market Stores

March 12, 2021

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Whole Foods Market is voluntarily recalling Cranberry Biscotti purchased from six stores in Maryland, Pennsylvania, and Virginia. The product is being recalled because it may contain undeclared Tree Nuts (Pistachio) that was not listed on the product label due to mislabeling. People who have an allergy or severe sensitivity to Tree Nuts (Pistachio) run the risk of a serious or life-threatening allergic reaction if they consume this product.
The affected products were sold in the Bakery department with sell-by dates through April 3, 2021 and can be identified by the PLU code 41712. The product was sold by weight in clear plastic containers. All affected product has been removed from store shelves. The issue was identified as a result of a customer complaint and one illness has been reported to date.
The affected product was sold at the following Whole Foods Market stores:
•    Whole Foods Market 10275 Little Patuxent Parkway, Columbia, MD 21044
•    Whole Foods Market 4420 Willard Avenue, Chevy Chase, MD 20815
•    Whole Foods Market 316 Kentlands Boulevard, Gaithersburg, MD 20878
•    Whole Foods Market 1575 The Fairway, Rydal, PA 19046
•    Whole Foods Market 111 Siena Drive, Upper Saint Clair, PA 15241
•    Whole Foods Market 4501 Market Commons Drive, Fairfax, VA 22033
Customers who purchased this product at Whole Foods Market can bring a valid receipt into the store for a full refund. Consumers with additional questions can call 1-844-936-8255 between the hours of 7:00 a.m. and 10:00 p.m. CST, Monday through Friday, or 8:00 a.m. and 6:00 p.m. Saturday through Sunday.

FSIS Issues Public Health Alert for Chicken Soup Product Due to Misbranding

March 12, 2021

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WASHINGTON, March 12, 2021 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to misbranding. The chicken soup product contains and declares wheat as an ingredient but has an incorrect statement of "gluten free" on the top label. FSIS is issuing this public health alert to ensure that consumers with allergic reactions to gluten are aware that these products should not be consumed. A recall was not requested because the affected products were produced and distributed among retail locations within the same corporate entity and sold directly to consumers.  It is believed that these products are no longer available to be purchased by consumers.
The ready-to-eat chicken noodle soup products subject to the public health alert are:
•    24-oz. plastic containers of “Signature CAFÉ Chicken Noodle Soup with White Meat Chicken” with best by dates of Apr. 27 21, May 2 21, May 8 21, and May 16 21.
The products bear establishment number “EST 46381” inside the USDA mark of inspection. This product was sold in retail locations in Alaska, Arizona, California, Hawaii, Idaho, Montana, Nevada, New Mexico, Oregon, Utah, Washington, and Wyoming.
The problem was discovered when one of the firm’s retail stores notified them of the issue. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers with food allergies who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Christine Wilcox, G.V.P. Communications, Albertsons Companies at christine.wilcox@albertsons.com.

MG Foods Recalls Various Turkey Sandwiches Due to Possible Listeria monocytogenes Contamination

March 10, 2021

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MG Foods of Charlotte, NC is recalling various Turkey Sandwiches due to a potential contamination of Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, a Listeria monocytogenes infection can cause miscarriages and stillbirths among pregnant women.
The products were distributed between March 3, 2021 and March 5, 2021 and packaged in clear plastic wedges & paper bags. The products were sold at distributors located at the Charlotte Douglas Airport and via vending machines and micro markets located in business locations in Georgia, North Carolina, South Carolina, and West Virginia. The company reacted swiftly and as of end-of-day March 5, 2021 affected products were removed from sale at all locations.
No illnesses have been reported to date.
On March 2, 2021 during routine environmental testing the company detected the presence of Listeria on surface areas where the recalled products were produced. Out of an abundance of caution, MG Foods is recalling the products due to the potential that some product may be contaminated with Listeria monocytogenes.
Products recalled at the Charlotte Douglas Airport are:
PRODUCT    SIZE    UPC    CONTAINER    USE BY DATES
MG Foods Combo Half & Half    6.82 oz    1 00000 50069 9    Plastic Wedge    3/9/2021
MG Foods Turkey & Cheddar BLT    6.9 oz    1 00000 50068 2    Plastic Wedge    3/7/2021
MG Foods Turkey & Swiss Croissant    7.5 oz    1 00000 50011 8    Brown Bag    3/7/2021
Products recalled in vending machines and micro markets located in Georgia, North Carolina, South Carolina and West Virginia are:
PRODUCT    SIZE    UPC    CONTAINER    USE BY DATES
Fresh to You Club on Toast    10.3 oz    MGF0930    Plastic Wrap    3/7/2021
Fresh to You Club Panini    8.50 oz    MGF9844    Plastic Wrap    3/7/2021
Fresh to You Club Sub    9.14 oz    C0932    Plastic Wrap    3/7/2021
Fresh to You Club Sub    9.14 oz    MGF9100    Plastic Wrap    3/7/2021
Fresh to You Deluxe Triple Decker Club    12.17 oz    MGF9719    Plastic Wrap    3/7/2021
Fresh to You Ham & Turkey Combo    5.85 oz    MGF3054    Plastic Wedge    3/9/2021
Fresh to You Ham & Turkey Combo on 12 Grain    7.20 oz    MGF6011    Plastic Wedge    3/9/2021
Fresh to You Jumbo Turkey & Cheese Sub    6.74 oz    MGF1002    Plastic Wrap    3/9/2021
Fresh to You Market Club    11.85 oz    MGF9800    Plastic Wrap    3/7/2021
Fresh to You Market Ham & Turkey Combo    5.85 oz    MGF23054    Plastic Wrap    3/9/2021
Fresh to You Market Shaved Turkey & Cheese    4.55 oz    MGF25571    Plastic Wedge    3/9/2021
Fresh to You Shaved Turkey & Cheese    4.55 oz    MGF5571    Plastic Wedge    3/9/2021
Fresh to You Turkey & Baby Swiss on a Honey Brown Roll    9.42 oz    MGF9703    Plastic Wrap    3/7/2021
Fresh to You Turkey & Cheddar Club    10.02 oz    MGF9710    Plastic Wedge    3/7/2021
Fresh to You Turkey & Cheese Cut    6.56 oz    MGF0596    Plastic Wedge    3/9/2021
Fresh to You Turkey & Cheese Hoagie    6.35 oz    MGF0597    Plastic Wrap    3/9/2021
Fresh to You Turkey & Sun-Dried Tomato Aioli on Pita    8.29 oz    MGF9806    Plastic Wrap    3/7/2021
Fresh to You Turkey & Swiss on a Kaiser Roll    8.1 oz    MGF9712    Plastic Wrap    3/7/2021
Fresh to You Turkey & Swiss on a Wheat Roll    5.22 oz    MGF0854    Plastic Wrap    3/9/2021
Fresh to You Turkey & Swiss on Whole Wheat    3.9 oz    MGF0283    Plastic Wedge    3/9/2021
Fresh to You Turkey Club Croissant    7.94 oz    MGF9103    Plastic Square    3/7/2021
Fresh to You Turkey Cranberry Pita    9.0 oz    MGF9804    Plastic Wrap    3/7/2021
Fresh to You Turkey Melt Croissant    6.7 oz    MGF3032    Plastic Wrap    3/9/2021
Fresh to You Tuscan Turkey Ciabatta    9.18 oz    MGF9810    Plastic Wrap    3/7/2021
MG Foods Combo Half & Half    6.82 oz    1 00000 50069 9    Plastic Wedge    3/9/2021
MG Foods The Club Sub    8.5 oz    1 00000 50002 6    Brown Bag    3/9/2021
MG Foods Turkey & Cheddar BLT    6.9 oz    1 00000 50068 2    Plastic Wedge    3/7/2021
MG Foods Turkey & Pepperjack Sub    7.9 oz    1 00000 50055 2    Brown Bag    3/7/2021
MG Foods Turkey & Provolone BLT    8.1 oz    1 00000 50065 1    Plastic Wedge    3/7/2021
MG Foods Turkey & Provolone on 12 Grain    8.9 oz    1 00000 50066 8    Plastic Wedge    3/7/2021
MG Foods Turkey & Swiss Croissant    7.5 oz    1 00000 50011 8    Brown Bag    3/7/2021
Product labels are attached for identification of products.
Consumers who have purchased these products are urged to discard any remaining product. Consumers may contact MG Foods at 1-855-424-8390 Monday thru Friday 7:00am – 7:00 pm EST for any questions related to this recall or to request a full refund.

Wilton Brands Issues Allergy Alert on Undeclared Milk in 7 Sprinkle Products

March 9, 2021

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Wilton Brands of Naperville, Illinois announced today a voluntary national recall of all lots of six sprinkles products and one kit containing affected sprinkles, because they may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious allergic reaction if they consume these products. 
A full list of recalled products with photos and SKUs, which were distributed nationally through retail stores, mail, order, and direct delivery, is as follows:
Product Name & Item #    Brand    Product Name & Item #    Brand
Tasty Coffee Shop Cookie Kit
Item # 1900-0-0054    Wilton/Tasty    Holiday Mix Sprinkles
Item # 710-7649    Wilton
Holiday Home Assorted Treat Toppings
Item # 710-0-0207    Holiday Home    Rainbow Chip Crunch Sprinkles
Item # 710-9704    Wilton
Valentine Chip Crunch Sprinkles
Item # 710-4277    Wilton    Assorted Treat Toppings Sprinkles
Item # 710-9722    Wilton
Rainbow Chip Crunch Sprinkles
Item #710-5364    Wilton          
This recall is being initiated because of one reported allergic reaction to date associated with one of the recalled products. Wilton is recalling all affected products with a similar formulation. The health and safety of our consumers is our primary concern and we are acting with the highest degree of caution and urgency to address this issue. Wilton has ceased production and distribution of the affected products. 
Consumers who have purchased these products should immediately dispose of them or return them to the place of purchase for a full refund.
These products will be removed from shelves at several retailers and distributors nationwide. A full list of retailers that have carried this product can be found at www.wilton.com/recallExternal Link Disclaimer.
For questions about the voluntary recall, please call our Consumer Care Hotline at 1-800-794-5866, Mondays thru Thursdays, 8 am to 4:30 pm CT, and Fridays, 8 am to 1 pm CT, or by sending an email to productrecall@wilton.com.

Mediterranean Food Inc. Recalls “Alqosh Sesame Oil” Because of Possible Health Risk

March 8, 2021

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Mediterranean Food Inc. of Warren, MI, is recalling its 2Lb plastic jar of "Alqosh Sesame Oil" because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
The recalled "Sesame Oil" were distributed in Michigan retail stores and distributors through our company's staff. The Product was distributed in the period from 11/06/2020 to 12/10/2020.
The product comes in a 2Lb, clear plastic jar marked with lot # 16082020 on the side of the jar and with a Production date of 08/16/2020 stamped on the side.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after routine testing by the Michigan Department of Agriculture and Rural Development (MDARD) at one of the retailers sold the product to which revealed the presence of Salmonella in some of the 2 Lb plastic jars of "Sesame Oil."
Production of the product has been suspended while FDA and the company continue their investigation as to the source of the problem.
Consumers who have purchased Alqosh Sesame Oil "Tahin" 2Lb plastic jar with lot # 16082020 should not consume the product and are urged to return them to the place of purchase for a full refund in the hours from 9:00Am to 4:00pm Monday to Friday. Consumers with questions may contact the company at 1-586-777-3460.

Hu Products Conducts Nationwide Voluntary Recall of Single Lot of 4 oz. Chocolate Covered Hunks - Sour Goldenberries Product Due to Undeclared Almonds

March 6, 2021

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Hu Products announced today a nationwide voluntary recall in the United States of a single production lot of the Hu Chocolate Covered Hunks - Sour Goldenberries Product (4 oz. bag) because some packages may contain undeclared almonds that were inadvertently added to the product during manufacturing. People who have an allergy or severe sensitivityto almonds run the risk of serious or life-threatening allergic reaction if they consume these products.
This recall is limited solely to the Hu Chocolate Covered Hunks - Sour Goldenberries Product (4 oz. bag), which was sold in retail stores and online in the United States. No other Hu products are affected, and this recall does not affect products in countries other than the United States.
The product being recalled is the following:
Product Description    Item UPC    Best By Date (found on top right of back label)    Lot Code
Hu Chocolate Covered Hunks - Sour Goldenberries Product, 4 oz. bag    850180006510    08/2021    202891
A picture of the consumer package is shown below.
We became aware of this issue as a result of a consumer contact. No reports of adverse reactions due to consumption of this product have been reported to the Company to date.
Consumers who have this product should not eat it and should discard any product they may have. Consumers should contact the company at 888-389-2224, Consumer Relations specialists are available Monday-Friday, 8 a.m. to 5 p.m. Central. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Contact:
Sal Brophy
+1-917-362-3272
Sally.Brophy@hukitchen.com
A photo accompanying this announcement is available at https://pr.globenewswire.com/FileDownloader/DownloadFile?source=pnr&fileGuid=344f324c-75b4-474e-ae7f-d82b181f3ccc

The Quaker Oats Company Issues Voluntary Recall of Quaker Rice Crisps Sweet Barbecue Flavor Due to Undeclared Soy Issue

March 4, 2021

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The Quaker Oats Company, a subsidiary of PepsiCo, Inc., today issued a voluntary recall for 3.03 oz. bags of Quaker Rice Crisps Sweet Barbecue Flavor because they may contain undeclared soy ingredients. 
People who have an allergy or severe sensitivity to soy run the risk of a serious or life-threatening allergic reaction if they consume the product contained inside the recalled bags. If you have purchased the impacted product, we advise you not to consume the product and urge you to dispose it. A total of 4,550 bags are being recalled with a specific best before date of May 29, 2021.
The products covered by this recall may have been distributed to retail stores in the following states: Alabama, Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Kansas, Louisiana, Missouri, Nebraska, New York, Nevada, North Carolina, Oregon, Tennessee, Utah, Virginia, and Washington. 
No other Quaker products or Rice Crisps bag sizes or flavors are impacted by this recall.
At this time, there are no reports of illness. Quaker has informed the FDA of the action.
Consumers with the product noted below can return the product to a retailer for a refund or contact Quaker Consumer Relations at 1-800-367-6287 (8:30 a.m. – 5:00 p.m. EST, Monday-Friday).
The specific recalled product information is listed below:
Product Description    Size    UPC    Best Before
Quaker Rice Crisps Sweet Barbecue Flavor    3.03 oz. Bags    0 30000 31984 0    MAY29213M21

El Abuelito EXPANDS Recall to Include Queso Fresco, Quesillo, and Requeson Products Because of Possible Health Risk

March 3, 2021

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El Abuelito Cheese of Paterson, NJ is recalling all Queso Fresco (Fresh, soft cheese), Quesillo (Oaxaca, string cheese), and Requeson (Ricotta) products, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria monocytogenes infection can cause miscarriages and stillbirths among pregnant women.
All Queso Fresco products with sell by dates through 032821; all Quesillo (Oaxaca, string cheese) products with sell by dates through 041621; and all Requeson (Ricotta) products with sell by dates through 031421 have been recalled. The products are sold as El Abuelito Cheese brand, distributed in CT, NJ, PA, NY; Rio Grande Food Products brand, distributed in VA, NC, MD; Rio Lindo distributed in NC and MD and Viejito, El Paisano, El Sabrosito, La Cima, Quesos Finos, San Carlos, and Ideal Brands.
The products were distributed through Feb 16, 2021 and were available in supermarkets, wholesale, and retails stores.
The following products being recalled were produced at Plant #34-12179 in the following form. Retailers may have repackaged the bulk Quesillo into smaller containers and sold this repackage product to consumers. This repackaged product may not bear the original labeling and product information as described below.
Quesillo
Brand    Product Name    Size    Container Type    UPC Code
El Abuelito Cheese    Quesillo Abuelito    12oz    Vacuum Pack    673130200000
    Quesillo Abuelito    5Lbs    Vacuum Bag Loose Bag    673130500001
    Quesillo Abuelito    10Lbs    Vacuum Bag Loose Bag    673130600008
El Viejito    El Viejito    10Lbs    Vacuum Bag Loose Bag    718122180950
El Paisano    El Paisano    5Lbs    Vacuum Bag    799456415468
    El Paisano    10Lbs    Vacuum Bag    799456415482
El Sabrosito    El Sabrosito    10Lbs    Vacuum Bag    749390337586
La Cima    La Cima    5Lbs    Vacuum Bag    072632891653
Quesos Finos    Quesos Finos    5Lbs    Vacuum Bag    851800004145
San Carlos    San Carlos    14Lbs    Loose Bag    814920000039
Ideal    Ideal    5Lbs    Vacuum Bag    610563082674
    Ideal    10Lbs    Vacuum Bag    897930001951
Requeson/Ricotta
Brand    Product Name    Size    Container Type    UPC Code
El Abuelito Cheese, Inc.    El Abuelito Requeson Ricotta    12oz    Clam Shell Container    673130300014
    El Abuelito Requeson Ricotta - Promocion $3.99    12oz.    Clam Shell Container    673130300014
El Viejito    El Viejito Requeson/Ricotta    12oz.    Clam Shell Container    718122180912
As of February 27, 2021, the CDC reports ten people infected with the outbreak strain of Listeria monocytogenes from four states.
El Abuelito has ceased the production and distribution of the product as FDA and El Abuelito continue their investigation as to what caused the problem.
As part of this outbreak investigation, the Connecticut Department of Public Health collected product samples of El Abuelito-brand Hispanic-style fresh and soft cheeses from a store where a sick person bought cheeses. On 2/19/2021, Whole Genome Sequencing (WGS) analysis conducted by the Connecticut State Laboratory determined that the Listeria monocytogenes found in the samples is a match to the outbreak strain.
Consumers who have purchased the stated Queso Fresco, Quesillo (Oaxaca, string cheese), and Requeson (Ricotta) products are urged not to consume and to return product to the place of purchase for a full refund. FDA recommends that anyone who purchased or received any El Abuelito brand Quesillo, Requeson, or recalled Queso Fresco cheeses use extra vigilance in cleaning and sanitizing any surfaces and containers that may have come in contact with these products to reduce the risk of cross-contamination. Listeria can survive in refrigerated temperatures and can easily spread to other foods and surfaces. Consumers with questions may contact El Abuelito Monday to Friday from 8 a.m. to 5 p.m. EST and Saturday from 8 a.m. to 12 p.m. EST at (973) 345-3503.
RETAIL DISTRIBUTION FOR El ABUELITO BRAND QUESO FRESCO, REQUESON, AND QUESILLO PRODUCTS
FDA has reason to believe that the following retail locations received the El Abuelito Brand Queso Fresco (Fresh, soft cheese) , Quesillo (Oaxaca, string cheese), and Requeson (Ricotta) that were included in the recall by El Abuelito. These cheese products may have been cut or repacked from their original packaging. This list may not include all retail establishments that have received the recalled product or may include retail establishments that did not actually receive the recalled product. Therefore, it is important that you use the product-specific identification information, available here, in addition to this list of retail stores, when you check the food you have to see if it has been recalled.

J&J Distributing (owned by New Harvest Foods) Recalls Multiple Products Because of Possible Health Risk

March 3, 2021

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J&J Distributing of St. Paul, MN, is recalling multiple products because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled products follow:
Brand / Retailer    DESCRIPTION    UPC    Code Date
Haug    Taco Tray 16 oz    6-10014-16383-9    3-Mar
Haug    Mini 7 Layer Dip Tray 22 oz    6-10014-16414-0    3-Mar
Haug    Taco Tray 16 oz    6-10014-16415-7    3-Mar
Haug    Taco Tray 29 oz    6-10014-16416-4    3-Mar
Fresh Thyme    Taco Dip 10oz    8-41330-12368    3-Mar
Tastebuds    Layered Fiesta Taco Dip 9 oz    0-38232-31611-8    3-Mar
Tastebuds    Taco Platter 26 oz    0-38232-31683-5    3-Mar
Tastebuds    Taco Platter 15.8 oz    0-38232-33235-4    3-Mar
Tastebuds    Taco Dip 9 oz    0-38232-31612-5    3-Mar
Earthgrown    Mini Taco Dip    6-10014-22341-0    3-Mar
Caribou    Turkey Sandwich 9 oz    7-98493-17447-5    26-Feb
Kwik Trip    Taco Dip 8oz    0-38232-36091-3    3-Mar
Kwik Trip    Taco Dip 15.8oz    0-38232-36090-6    3-Mar
The recalled products were distributed nationwide in retail stores.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after routine testing by the company revealed the presence of Listeria monocytogenes in a utensil used to produce the products.
Consumers who have purchased any of the affected products are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 651-221-0560, Monday through Friday, 7 am to 5 pm.

Milky Way International Trading Corp. Recalls Canned Corned Beef Products Imported Without Benefit of Inspection

March 1, 2021

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WASHINGTON, March 1, 2021, Milky Way International Trading Corp., doing business as MW Polar, a Norwalk, Calif., firm, is recalling approximately 297,715 pounds of ready-to-eat canned corned beef products that were imported and distributed in the United States without the benefit of FSIS import re-inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. This is considered a Class 1 Recall; Health Risk High.
The canned corned beef items were imported on various dates between June 6, 2020 to Jan. 21, 2021. The product cans are labeled with various “Best Before” dates and the product cases are labeled with various shipping marks. The affected codes can be found on the following chart.[View Product Labels (PDF only)]
The products subject to recall bear “Australia Inspected” number “39” and were shipped to retail locations nationwide.
The problem was discovered after FSIS received a tip from an industry representative indicating that corned beef product received from Milky Way did not undergo FSIS import reinspection.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.  
FSIS is concerned that some product may be in consumers’ pantries or in their refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers with questions about the recall can contact Ramita Garviso, MW Polar Consumer Relations Specialist, at info@mwpolar.com and (562) 921-2800, Ext. 160. Members of the media with questions about the recall can contact Ruby Jing, MW Polar Vice President of Pricing and Marketing, at Ruby129@mwpolar.com and (562) 921-2800, Ext. 129.

FSIS Issues Public Health Alert for Beef Meatball Products Due to Misbranding and Undeclared Allergen

March 1, 2021

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WASHINGTON, Feb. 25, 2021 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert because Whole Foods Market, Inc., sold an undetermined amount of beef meatballs with marinara sauce that were misbranded and were produced with an undeclared allergen. The products contain parmesan cheese made from milk, which is a known allergen, and is not declared on the product label. FSIS is issuing this public health alert out of the utmost of caution to ensure that consumers with allergic reactions to milk are aware that these products should not be consumed. A recall was not requested because it is believed that the affected products are no longer available to be directly purchased by retail consumers.
The beef meatballs with marinara sauce products subject to the public health alert are:
•    24-oz. clear plastic containers of “Whole Foods Market Beef Meatballs with Marinara” with a PLU code of 39496 and sell-by dates through 2/27/21.
This product was sold in retail locations in Illinois, Indiana, Iowa, Kentucky, Michigan, Minnesota, Missouri, Ohio and Wisconsin.
The problem was discovered when the firm notified FDA of a customer report of an adverse reaction due to consumption of the product. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers with food allergies who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions about the public health alert can contact Nathan Cimbala, Global Public Relations, Whole Foods Market, Inc., at nathan.cimbala@wholefoods.com.

J&J Distributing Recalls Ready-to-Eat Meat and Poultry Salads and Wrap Products Due to Possible Listeria Contamination

February 26, 2021

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WASHINGTON, Feb. 26, 2021 – J&J Distributing, a St. Paul, Minn., establishment, is recalling approximately 33 pounds of ready-to-eat meat and poultry salads and wrap products that may be adulterated with Listeria monocytogenes (Lm), the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.  Class 1 Recall; Health Risk: High
The fully cooked, not shelf stable salads and wraps were produced and packaged on Feb. 23, 2021 and list a “Sell-by” date of Feb. 28, 2021 on the packaging label. The following products are subject to recall: [View Labels (PDF Only)]:
•    9-oz. plastic container of “COBB SALAD” on the product label.
•    10-oz. plastic container of “Because life is delicious. tastebuds Bacon Lettuce Avocado Tomato Wrap” on the label.
•    10-oz. plastic container of “Because life is delicious. tastebuds Turkey Ranch Club Wrap” on the label.
•    10-oz. plastic container of “Because life is delicious. tastebuds Chicken Caesar Wrap” on the label.
•    12-oz. plastic container of “Because life is delicious. tastebuds Southwest Style Chicken Salad” on the label.
•    12-oz. plastic container of “Southwest Style Chicken Salad” on the label.
The products subject to recall bear establishment number “EST. 38450” inside the USDA mark of inspection. These items were shipped to retail locations in Minnesota and Wisconsin.
The problem was discovered when the firm received confirmation from their third-party lab that a product contact surface sample returned positive for Lm.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
Consumption of food contaminated with Lm can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery, or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

Urban Remedy Voluntarily Recalls Beverages with Undeclared Almond & Cashew Allergens

February 22, 2021

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Urban Remedy, a California-based producer and retailer of ultra-fresh, organic meals, is voluntarily recalling 462 beverages because it may contain undeclared almonds and cashews. People who have an allergy or severe sensitivity to almonds and cashews run the risk of serious or life-threatening allergic reaction if they consume these products.
“In an abundance of caution, we are voluntarily recalling a limited number of our products that contain potentially undeclared allergens,” said Paul Coletta, the company’s CEO. “We’re taking preventative action to keep our customers safe, although no customer complaints have been reported.”
The recall was initiated after it was discovered that products containing almond and cashew was distributed in packaging that did not reveal the presence of the above-mentioned allergens. Almond Maca is labeled to contain Almonds but due to mislabeling contains Cashews Cacao Mocha is labeled to contain cashews but due to the mislabeling actually contains Almonds. Because the allergen labeling was involved and consumption by an allergic individual could result in a serious health issue, Subsequent investigation indicates the problem was caused by a temporary breakdown in the company’s production and packaging process.
Products were distributed on the following states and cities:
California:
•    Larkspur
•    Berkeley
•    Mill Valley
•    San Rafael
•    Lafayette
•    San Francisco
•    Los Gatos
•    Solana Beach
•    Venice
•    Mountain View
•    San Mateo
•    Concord
•    Oakland
•    Fairfax
•    Sausalito
•    San Anselmo
•    Danville
•    Fair Oaks
•    Ferndale
•    San Bruno
•    Richmond
•    Antioch
•    Plymouth
•    Redondo Beach
•    Greenbrae
The products were sold in Urban Remedy’s retail stores, online, and at other California retailers. All remaining affected products have been removed from store shelves and the Urban Remedy website.
“All of the potentially affected products have a use-by date of 3/11/2021,” said Coletta. “If you purchased any of these products, please don’t drink them if you any kind of reaction to these allergens – throw them out or return them to the store for a full refund.”
List of contaminated products:
Item Name    UPC Item Code    Use-By Date    Product Size    Quantity
Almond Maca    813377021093    3/11/2021    16oz    184
Cacao Mocha    813377021093    3/11/2021    16oz    278
Consumers with additional questions can call (855) 875-8423.

News Release GLG Trading Inc., Recalls Beef Tallow Products Imported Without the Benefit of Inspection

February 22, 2021

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GLG Trading Inc., a Chino, Calif. establishment, is recalling (Class 1 Recall; Health Risk-High) approximately 96,810 pounds of beef tallow products that were imported from the People’s Republic of China, an ineligible country for beef, without the benefit of FSIS import re-inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The following heat-treated shelf stable Hotpot Seasoning items containing beef tallow are subject to recall: [View Labels (PDF Only)]:
•    17.6-oz. vacuumed sealed packages of “Ming Yang Hotpot Seasoning (Slightly spicy).”
•    17.6-oz. vacuumed sealed packages of “Ming Yang Hotpot Seasoning (Super spicy, Extremely).”
•    12.07-oz. vacuumed sealed packages of “Ming Yang Hotpot Seasoning (Medium spicy, Mala).”  
The products subject to recall do not bear a Federal mark of inspection. These items were shipped to distributors, retail locations and restaurants in Arizona, California, Hawaii, Nevada, New York and Texas.                                 
The problem was discovered during verification activities.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.  
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Derek Yang, Secretary, at (805) 366-6666.

El Abuelito Recalls Queso Fresco Products Because of Possible Health Risk

February 19, 2021

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El Abuelito Cheese of Paterson, NJ is recalling all Queso Fresco (Fresh, soft cheese) products, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria monocytogenes infection can cause miscarriages and stillbirths among pregnant women.
All Queso Fresco products with sell by dates through 032821, have been recalled. The products are sold as El Abuelito Cheese brand, distributed in CT, NJ, PA, NY; Rio Grande Food Products brand, distributed in VA, NC, MD; and Rio Lindo distributed in NC and MD. The products were distributed through Feb 16, 2021 and were available in supermarkets, wholesale, and retails stores.
The following products being recalled were produced at Plant #34-12179 in the following forms
Brand    Product Name    Size    Container Type    UPC Code
El Abuelito Cheese    Queso Fresco Regular    12 oz.    Plastic Container    673130100003
    Queso Fresco Promoción    10 oz.    Plastic Container    673130100078
    Queso Fresco de Hoja    12 oz.    Plastic Container    673130100065
    Queso Fresco    5 Lb.    Vacuum Packed    673130100058
    Queso Fresco Guatemala    12 oz.    Plastic Container    673130100027
Rio Grande Food Products, Inc.    Chirilagua Queso de Hacienda    12 oz.    Plastic Container    738529005571
    Queso Fresco Campestre con Hoja    14 oz.    Plastic Container    812324031161
    Queso Fresco Campestre Artesanal    14 oz.    Plastic Container    738529002518
    Queso Fresco con Hoja    14 oz.    Plastic Container    738529004581
    Queso Fresco Yorito    12 oz.    Plastic Container    738529005564
    Queso Fresco Olancho    14 oz.    Plastic Container    812324031222
    Cuajada Fresca Guatemalteca    12 oz.    Plastic Container    738529001276
    Cuajada Fresca Hondureña    12 oz.    Plastic Container    738529001269
    Cuajada Fresca Salvadoreña    12 oz.    Plastic Container    738529001252
Rio Lindo    Queso Fresco Mexicano    12 oz.    Plastic Container    718122088587
    Queso Fresco Hondureño    12 oz.    Plastic Container    718122088591
    Queso Fresco Salvadoreño    12 oz.    Plastic Container    718122088607
As of February 11, 2021, the CDC reports seven people infected with the outbreak strain of Listeria monocytogenes from four states.
El Abuelito has ceased the production and distribution of the product as FDA and El Abuelito continue their investigation as to what caused the problem.
As the FDA stated, about this outbreak investigation, the Connecticut Department of Public Health collected product samples of El Abuelito-brand Hispanic-style fresh and soft cheeses from a store where a sick person bought cheeses. Sample analysis showed the presence of Listeria monocytogenes in samples of El Abuelito Queso Fresco sold in 10 oz packages, marked as Lot A027 with an expiration date of 02/26/2021. Samples are currently undergoing Whole Genome Sequencing (WGS) analysis to determine if the Listeria monocytogenes found in these samples is a match to the outbreak strain. At this time, there is not enough evidence to determine if this outbreak is linked to El Abuelito Queso Fresco.
Consumers who have purchased the stated Queso Fresco products are urged not to consume and to return product to the place of purchase for a full refund. Consumers with questions may contact directly El Abuelito Monday to Friday from 8 a.m. to 5 p.m. EST and Saturday from 8 a.m. to 12 p.m. EST at (973) 345-3503.

Market District Voluntarily Recalls Gourmet Chocolate Covered Pretzels Due to Undeclared Pecan Allergen

February 19, 2021

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Giant Eagle, Inc. has issued a voluntarily recall of Market District Gourmet Pretzel Platters and Gourmet Pretzel Bags due to the possibility the product may contain an undeclared pecan allergen. Those who have an allergy or severe sensitivity to pecans could experience a serious or life-threatening allergic reaction if they consume these products.
The impacted products have “sell by” dates through 04/03/21 and can be identified by PLUs 25206 and 45505 located in the upper right corner of the item’s scale tag. The recalled items were sold in the Sweet Shoppe department in the Township of Pine Market District and the Settler’s Ridge Market District in Pennsylvania and the Portage Crossing Market District in Ohio.
Giant Eagle was made aware of the issue by a guest who purchased the product, and the company has since learned that the cause was due to an error in packaging at the store. To date, there has been one reported illness associated with this recall.
Customers who have purchased the affected product should dispose of it and return a qualifying receipt local Giant Eagle or Market District store for a refund. Customers with questions may call Giant Eagle Customer Care at 1-800-553-2324 Monday through Friday 9 a.m. to 9 p.m. EST.
In addition to this public communication regarding this recall, Giant Eagle initiated its consumer recall telephone notification process. The consumer recall process uses purchase data and consumer telephone numbers housed in the Giant Eagle Advantage Card database to alert those households that purchased the affected product and have updated telephone contact information in the database.

AH Company International Distribution, Inc., Recalls Pork Products Imported Without the Benefit of Inspection

February 19, 2021

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WASHINGTON, Feb. 19, 2021 – AH Company International Distribution Inc., a Garden Grove, Calif. firm, is recalling approximately 30,081 pounds of pork pâté products that were imported from an ineligible establishment and distributed in the United States without the benefit of FSIS import re-inspection.
The following heat-treated shelf stable pork pâté items are subject to recall: [View Labels (PDF only)]
•    240-gram cans of Monique Ranou Pâté de Foie
•    240-gram cans of Monique Ranou Pâté de Campagne
•    180-gram jars of Monique Ranou Pâté de Campagne Supérieur
The products subject to recall bear the French establishment number “FR 56-246-008 CE”, an ineligible establishment. These items were shipped to distributor locations nationwide.
The problem was discovered during routine FSIS verification activities.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider. 
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Quynh Nguyen, AH Company International Distribution Inc., Secretary, at (779) 772-2354 or nguyenky_ngocquynh@yahoo.com.vn

Aaron’s Gourmet Smoked Fish Recalls Smoked Fish Products Produced Without Licensure and Regulatory Oversight

February 18, 2021

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Aaron’s Gourmet Smoked Fish is issuing a voluntary recall of all smoked fish products due to the lack of licensure and regulatory oversight by the state agency. The products are packaged in both glass jars and vacuum-packed plastic bags.
The products were distributed to Growers Outlet and Berry Good PDX in Portland, Oregon. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase for a full refund.
The products have been voluntarily recalled by Aaron’s Gourmet Smoked Fish. We are not aware of any reported cases of illness related to these products.
This recall is being made with the knowledge of the Oregon Department of Agriculture.
Please contact Aaron at 503-372-9849 for questions or complaints.

Russ Davis Wholesale Issues Allergy Alert on Undeclared Fish (Anchovies) in Kowalski’s Buffalo Cauliflower Bites

February 15, 2021

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Russ Davis Wholesale of Wadena, Minnesota is voluntarily recalling Kowalski’s brand Buffalo Cauliflower Bites with Kowalski’s Steakhouse Blue Dressing because the Blue Cheese Dressing contains undeclared fish (anchovies).  People who have an allergy or severe sensitivity to fish (anchovies) run the risk of serious or life-threatening allergic reaction if they consume this product.
Kowalski’s brand Buffalo Cauliflower Bites with Kowalski’s Steakhouse Blue Dressing 22 oz was distributed to 7 metro Kowalski’s stores located in Minnesota.  Product with Use By Dates of 1/19/2021 through 2/10/21 are impacted by this Recall.
No illnesses have been reported to date.
The recall was initiated after it was discovered that the blue cheese dressing containing fish (anchovies) was distributed in packaging that did not reveal the presence of fish (anchovies).
Consumer who purchased Kowalski’s brand Buffalo Cauliflower Bites with Kowalski’s Steakhouse Blue Dressing with fish (anchovy) allergies should not consume this product, and direct questions to Customer Service at 1-877-433-2173.

Litehouse Inc. Issues Allergy Alert on Undeclared Anchovies in Product

February 15, 2021

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Litehouse Inc. is voluntarily recalling a limited quantity of its Brite Harbor Caesar Dressing & Dip 1.5 oz pillows because it may contain undeclared anchovies. The Food and Drug Administration has been made aware of this recall which is limited to one production day from a single manufacturing location.
Litehouse took this action proactively because people who are sensitive or have allergies to anchovies could be at risk of an adverse reaction if they consume this product. No reports of adverse reactions due to consumption of this product have been reported. Anyone concerned about a reaction should contact a healthcare provider.
In total, 225 cases of 60/1.5 oz Brite Harbor Caesar pouches were distributed to a limited number of customers in Washington, Oregon, Idaho, and Utah.  All customers impacted by this voluntary recall have been notified. The ‘Best Used By’ date can be found on the back of the pillow, labeled: 03 071321 with the lot code of 03 071321 16002 60/1.5 oz Brite Harbor Caesar. No other code dates of this product or any other Litehouse products are involved in this recall.
The voluntary recall was initiated after it was discovered that product labeling stated Caesar on the Front label and Blue Cheese on the back. Subsequent investigation indicates the problem was caused by a packaging error. Consumers who have purchased the affected product are asked to return them to the place of purchase for a full refund. Consumers with questions may contact Litehouse customer service at 1-800.578.1652 or litehousefoods.com/contact

Dole Fresh Vegetables, Inc. Is Voluntarily Recalling Two Lot Codes of Dole™ Sunflower Crunch Chopped Salad Kit

February 10, 2021

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Dole Fresh Vegetables, Inc. is voluntarily recalling two lot codes of Dole™ Sunflower Crunch Chopped Salad Kit.
Description    UPC    Best If Used by Date    Lot Code
Dole™ Sunflower Crunch Chopped Salad Kit    0-71430-00034-2    02-11-21    W02702A
W02702B
This recall is due to possible undeclared allergens (wheat and tree nuts) in Dole™ Sunflower Crunch Chopped Salad Kit. The dressing and topping kit (masterpack) designed for a different Dole product was unintentionally used during a portion of the production of the salad. Dole Fresh Vegetables, Inc. is coordinating closely with regulatory officials. No illnesses nor allergic reactions have been reported to date in association with the recall. However, people who have an allergy to wheat and tree nuts may have a serious or life-threatening allergic reaction if they consume this product.
The product lot code and Best if Used by Date are located on the upper right corner of each bag and the UPC code is located on the bottom right corner of the back of each bag. The impacted products were distributed in OH, NY and WI. Consumers are advised to check product they have in their homes and discard any product matching the production description, UPC codes, product lot code and Best if Used by Date listed above.
No other Dole products are included in the recall. Only Dole™ Sunflower Crunch Chopped Salad Kit with the exact UPC code, lot code and Best if Used by Date identified above are included in the recall. Consumers who have any remaining product should not consume it, but rather discard it. Retailers and consumers with questions may call the Dole Consumer Center at 1-800-356-3111, which is open 24 hours a day.

Delicae Gourmet LLC Issues Allergy Alert on Undeclared Shrimp Allergen in Thai Peanut Sauce, Panang Curry Sauce, and Spicy Red Curry Sauce

February 9, 2021

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Delicae Gourmet LLC of Tarpon Springs, FL is recalling Thai Peanut Sauce, Panang Curry Sauce, and Spicy Red Curry Sauce, because it contains undeclared shrimp allergen.  People who have an allergy or severe sensitivity to shrimp run the risk of serious or life-threatening allergic reaction if they consume these products.
Thai Peanut Sauce, Panang Curry Sauce, and Spicy Red Curry Sauce was distributed to retail stores in the following areas: Springfield, MO; Crystal Lake, IL; Palisade, CO; Colorado Springs, CO; Long Lake, NY; Long Grove, IL; Sheridan, WY; Venice, FL; Pittsburgh, PA; Nassawadox, VA.
The three products are packed in 12 oz. glass bottles with green shrink wraps on the necks. The brand name is Delicae Gourmet and the flavors are:
-Thai Peanut UPC code #643558406919
Batch No. 20175; best by date: October 13, 2023
Batch No. 20138; best by date: August, 26 2023
Batch No. 20068; best by date: May 5, 2023
Batch No. 19419; best by date: September, 19 2022
Batch No. 19276; best by date: July 10, 2022
Batch No. 19196; best by date: May 30, 2022
Batch No. 19148; best by date: April 17, 2022
Batch No. 19040 best by date: February 6, 2022
Batch No. 18226; best by date: December 1, 2021
Batch No. 18039; best by date: March 1, 2021
-Panang Curry UPC code #643558406711
Batch No. 20205; best by date: November 8, 2023
Batch No. 19484; best by date: October 30, 2022
Batch No. 19096; best by date: March 18, 2022
Batch No. 18225; best by date: December 1, 2021
Batch No. 18108; best by date: July 2, 2021
-Spicy Red Curry UPC code #643558406810
Batch No. 20084; best by date: May 28, 2023
Batch No. 19404; best by date: September 10, 2022
Batch No. 19158; best by date: April 25, 2022
Batch No. 18213; best by date: November 19, 2021
No illnesses have been reported to date.
The recall was initiated after it was discovered that product containing shrimp was distributed in packaging that did not reveal the presence of the shrimp. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's production and packaging processes.
Consumers who have purchased the Delicae Gourmet products mentioned are instructed to return it to the place of purchase for a full refund. Consumers with questions may contact Delicae Gourmet at 1-800-942-2502.
Phones will be manned from 9AM to 5PM Eastern Time Zone, Monday thru Friday.

Hickory Harvest Foods Issues Allergy Alert on Undeclared Almonds in Sprouts Vanilla Flavored Yogurt Covered Cranberries

February 9, 2021

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Hickory Harvest Foods of Akron, OH is recalling Vanilla Flavored Yogurt Covered Cranberries manufactured under the brand of Sprouts Farmers Market because they may contain undeclared Almonds.  People who have an allergy or severe sensitivity to Almonds run the risk of serious or life- threatening allergic reaction if they consume these products.
Product was sold by select Spouts Stores in Texas, Arizona, New Mexico, Kansas, Oklahoma, Missouri, California, Colorado, Alabama, Tennessee, Nevada, Utah, Georgia, North Carolina, South Carolina, and Florida between June 2, 2020 to February 2, 2021.
The product is packaged in 12 oz bags under the Sprouts Farmers Market brand, Vanilla Flavored Yogurt Covered Cranberries, Best By Date 5/28/21 stamped on the top right corner of the backside of the package, UPC 646670463778.  No other Best By Dates of this product are affected.
No illnesses have been reported to date.
The recall was initiated after it was discovered that product containing Almonds may have been distributed in packaging that did not reveal the presence of Almonds.
Consumers who have purchased the product are urged to return it to the place of purchase for a refund.  Consumers with questions may contact Hickory Harvest Foods at (330) 644-6266, Monday through Friday, 8:00 am to 4:30 pm EST.
Hickory Harvest Foods
90 Logan Parkway
Akron, OH  44319

Ocean Beauty Seafood LLC Issues Allergy Alert on Undeclared Soy in Publix Brand Parmesan-Crusted Wild Alaskan Salmon Fillets 12 Oz. Package

February 8, 2021

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Ocean Beauty Seafood LLC of Seattle, WA is recalling 8450 packages of Publix brand Parmesan-Crusted Wild Alaskan Salmon Fillets, net wt.12oz, frozen, UPC 41415 30245 7, because it may contain undeclared soy due to mis-packaging. People who have an allergy or severe sensitivity to soy run the risk of serious or life-threatening allergic reaction if they consume this product.
The affected Parmesan-Crusted Wild Alaskan Salmon Fillets retail box bears the code date “Best Before/Use By date 021122”, and the affected Teriyaki sauced product is observed through a clear inner vacuum package inside the retail box. Images of the affected and non-affected product are found below.
The affected product was distributed directly to Publix Super Markets Inc distribution warehouses located in Florida and Georgia between 9/18/20 and 11/4/20. Publix further distributed product to their various retail stores in the southeast.
The problem was discovered when a consumer reported that the Teriyaki sauced salmon was found inside the retail box labeled as Parmesan-crusted salmon. Further investigation by the co-packer UniSea Cold Storage of Redmond, WA revealed that the that the loading box machine operator must have inadvertently grabbed the Parmesan-crusted salmon retail box instead of the correct boxes. We estimate only 300 units of 8450 Teriyaki sauced salmon packages were mis-packaged as Parmesan-Crusted Wild Alaskan Salmon Fillets.
There have been no adverse/allergic reactions reported to date.
This recall is being made with the knowledge of, and in cooperation with, the U.S. Food and Drug Administration.
Consumers that find any affected product as described in this recall notice are asked to either dispose of the product or return the product to the point of purchase for a refund. Consumers with questions may contact the company at 206-286-2566 from 7am to 4pm PST, Monday through Friday. Or via email to info@oceanbeauty.com.

Shenandoah Growers, Inc Issues a Limited, Voluntary Recall of Specific Imported Organic Basil Because of Potential Health Risk

February 8, 2021

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Shenandoah Growers, Inc (Harrisonburg, VA) out of an abundance of caution, has issued a limited, voluntary recall of approximately 3240 units of branded fresh cut, packaged organic basil clamshells packed at its Indianapolis, Indiana location due to a possible health risk from Cyclospora.
Cyclosporiasis is an intestinal infection caused by the Cyclospora parasite. A person may become infected after ingesting contaminated food or water. Common symptoms include severe abdominal pain, watery diarrhea, nausea and vomiting, body aches and fatigue. The infection is treated with antibiotics and most people respond quickly to treatment.
Only the following specific lot codes are affected:
PV40515 1034     PV40515 3034     PV40515 4034     PV40515 3035
The affected product has a country of origin of Colombia and was harvested entirely from Puerto Vallarta Herbs SAS (Farm) and imported by Vallarta Organics LLC dba Organic Destiny (Importer).
Affected lot codes shipped:
Lot Code:    Pack Date:    Brand:    Size:    Location    UPC:
PV40515 1034    2/3/2021    Shenandoah Growers by That’s Tasty    0.75 oz    Indianapolis Fruit    7-68573-00101-4
PV40515 1034    2/3/2021    Shenandoah Growers by That’s Tasty    2.0 oz    Indianapolis Fruit    7-68573-02143-2
PV40515 1034    2/3/2021    Shenandoah Growers by That’s Tasty    4.0 oz    Indianapolis Fruit    7-68573-00141-0
PV40515 3034    2/3/2021    That’s Tasty (Pasta Blend)    0.5 oz    Vine Line Produce    7-68573-52008-9
PV40515 3034    2/3/2021    That’s Tasty    0.5 oz    Vine Line Produce    7-68573-50502-4
PV40515 3034    2/3/2021    Shenandoah Growers by That’s Tasty    4 oz    Vine Line Produce Bulk    N/A
PV40515 3034    2/3/2021    Shenandoah Growers by That’s Tasty    1 lb.    Vine Line Produce Bulk    N/A
PV40515 4034    2/3/2021    Simple Truth    3.0 oz    Kroger    0-11110-00876-3
PV40515 1034    2/3/2021    That’s Tasty    0.25 oz    J&J Distributing    7-68573-02515-7
PV40515 1034    2/3/2021    Shenandoah Growers by That’s Tasty    0.75 oz    J&J Distributing    7-68573-00101-4
PV40515 3035    2/4/2021    That’s Tasty    3.0 oz    Schnucks    7-68573-53001-9
Recalled products were distributed to select retail stores between 2/3/2021 to 2/4/2021 in the following states: Illinois, Indiana, Iowa, Michigan, Minnesota, Mississippi, Missouri, Ohio, Tennessee, and Wisconsin.
This recall notification is being issued due to a single instance in which a sample of bulk product was pulled at the port of entry in Miami and tested by the FDA as part of routine surveillance and indicated the potential presence of Cyclospora.
Affected Shenandoah Growers customers have been notified of the recall and instructed to immediately remove and discard recalled products from all store shelves, distribution and other inventories to ensure they are no longer available for sale or consumption.
The Shenandoah Growers recall includes only those clamshells of certified organic basil clearly marked with the affected lot codes listed above. The lot code can be found printed on each clamshell.
No other Shenandoah Growers products are subject to recall, and the company has no knowledge of any illness reported or related to this product to date.
Consumers who may have a recalled basil product should discard it immediately and not eat it. Consumers with questions, or to obtain refunds, may contact the Shenandoah Growers Consumer Response Center at 844-896-6939 Monday through Friday, 8 am to 5 pm EST.
Shenandoah Growers takes food safety matters very seriously, and stringently follows all mandated regulations and implements preventive measures designed to minimize potential risks. Shenandoah Growers is working in close coordination with regulatory officials, including the FDA, on this matter.
Company Contact Information
Shenandoah Growers Consumer Response Center
844-896-6939

Food Evolution Recalls Ready-to-Eat Dip and Salad Products Containing Meat Produced Without Benefit of Inspection

February 5, 2021

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WASHINGTON, Feb. 5, 2021 – Food Evolution, a Schiller Park, Ill. establishment, is recalling approximately 6,806 pounds of ready-to-eat (RTE) dip and salads products containing meat that were produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. 
The RTE dip and salad items containing meat were produced on various dates from Nov. 9, 2020, through Jan. 29, 2021 and have “USE BY” dates through Feb. 6, 2021. The following products are subject to recall: [View Labels (PDF only)]
•    31-oz. container containing “Taco Dip With Refried Beans, Chili, Sour Cream, Cheddar, Onions, Black Olives, Jalapenos, & Red Pepper thoughtfully handmade —fresh to you — Fresh, Fast, Gourmet.”
•    18-oz. container containing “Taco Dip With Refried Beans, Chili, Sour Cream, Cheddar, Onions, Black Olives, Jalapenos, & Red Pepper thoughtfully handmade —fresh to you — Fresh, Fast, Gourmet.”
•    7-oz. container containing “Tri-Colored Italian Style Rotini Pasta Salad with Salami thoughtfully handmade — fresh to you — Fresh, Fast, Gourmet.”
•    8-oz. container containing “German Style Potato Salad with Bacon thoughtfully handmade — fresh to you — Fresh, Fast, Gourmet.”
The products subject to recall bear establishment number “EST. 34309” inside the USDA mark of inspection. These items were shipped to retail locations in Illinois.
The problem was discovered during routine FSIS verification tasks. FSIS personnel discovered that the establishment produced amenable product at an off-site facility without the benefit of federal inspection, then repackaged and labeled the products with the USDA mark of inspection at the federal establishment.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Art Sezgin, President of Food Evolution, at (818) 837-7600. 

Dole Fresh Vegetables Announces Limited Voluntary Recall of Dole™ Endless Summer Salad Kit Due to Undeclared Allergens

January 29, 2021

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Dole Fresh Vegetables, Inc. is voluntarily recalling a single lot code of Dole™ Endless Summer Salad Kit.
Description    UPC    Best If Used by
Date    Lot Code
Dole™ Endless Summer Salad Kit    0-71430-01073-0    01-26-21    B00912A
B00912B
This recall is due to possible undeclared allergens (fish and egg) in Dole™ Endless Summer Salad Kit. The dressing and topping kit (masterpack) designed for a different Dole product was unintentionally used during a portion of the production of the salad. Dole Fresh Vegetables, Inc. is coordinating closely with regulatory officials. No illnesses nor allergic reactions have been reported to date in association with the recall. However, people who have an allergy to fish or eggs may have a serious or life-threatening allergic reaction if they consume this product.
The product lot code and Best if Used by Date is located on the upper right corner of each bag and the UPC code is located on the bottom right corner of the back of each bag. The impacted products were distributed in AZ, CA, CO, IA, ID, IL, KS, MN, MS, ND, OK, OR, PA, TX, UT, WA, and WI. Consumers are advised to check product they have in their homes and discard any product matching the production description, UPC codes, product lot code and Best if Used by Date listed above.
No other Dole products are included in the recall. Only Dole™ Endless Summer Salad Kit with the exact UPC code, lot code and Best if Used by Date identified above, are included in the recall. Consumers who have any remaining product should not consume it, but rather discard it. Retailers and consumers with questions may call the Dole Consumer Center at 1-800-356-3111, which is open 24 hours a day.

Hong Thai Foods Corp Issues Allergy Alert on Undeclared Milk Allergens in Golden Boy Custard Muffin Banana

January 28, 2021

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Hong Thai Foods Corp. of Brooklyn, NY is recalling its 220 grams/7.76 ounce packages of Golden Boy Custard Muffin Banana because they may contain undeclared milk allergens. Consumers who are allergic to milk allergens may run the risk of serious or life-threatening allergic reactions if they consume this product.
The recalled Golden Boy Custard Muffin Banana were distributed nationwide in retail stores. The product comes in a 220 grams/7.76 ounce, rigid clear plastic package marked with Best Before date of 29/01/2022 on the bottom. The product UPC code is 9555719731598.
No illnesses or allergic reactions involving this product have been reported to date.
The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of undeclared milk allergens in the 220 grams/7.76 ounce packages of Golden Boy Custard Muffin Banana which did not declare a milk ingredient on the label.
Consumers who have purchased 220 grams/7.76 ounce packages of Golden Boy Custard Muffin Banana are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at (718) 237-1511.

Think! and Interpac Technologies, Inc., Issue Voluntary Recall and Allergy Alert on Undeclared Tree Nuts in Think! Protein + Fiber Oatmeal, Farmer’s Market Berry Crumble Products

January 28, 2021

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think! and Interpac Technologies, Inc., of Woodland, California, a supplier of certain think! brand oatmeal products, have issued a voluntary recall on specific lots of think! Protein + Fiber Oatmeal, Farmer’s Market Berry Crumble products which may inadvertently contain undeclared tree nuts, including almonds and pecans. People who have an allergy or severe sensitivity to tree nuts, such as almonds and pecans, run the risk of serious or life-threatening allergic reaction if they consume the recalled products.
The recalled think! Protein + Fiber Oatmeal, Farmer’s Market Berry Crumble products were manufactured in the United States, distributed nationwide and reached consumers through retail stores and ecommerce websites, including www.thinkproducts.comExternal Link Disclaimer.
The recalled products are sold in individual 1.76 oz bowls with a UPC Code of 753656711836 or a case containing 6 individual bowls with a UPC Code of 753656712338, all with best by dates of N15OCT21, N16OCT21, N19OCT21, N20OCT21, or N21OCT21 stamped on the bottom of the bowl.
To date, neither Interpac Technologies nor think! have received any reports of illness associated with consumption of the recalled products. All of the affected products include the following statement on the packaging: “MADE IN A FACILITY THAT PROCESSES…TREE NUTS.”
The recall was initiated following a report from a consumer of finding a piece of almond while consuming the product, and it was discovered that products manufactured in the same lot may contain undeclared almonds or pecans. Subsequent investigation indicates the problem was caused by an inadvertent error in the production process.
Consumers who have purchased the products under recall should not eat them and may return them to the place of purchase for a full refund. For additional information, consumers may call 866-98THINK from 8:30 – 5:00 pm CST.

Maine Grains, Inc. Issues Allergy Alert on Undeclared Soy in Organic Yellow Peas

January 27, 2021

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Maine Grains, Inc. of Skowhegan, Maine is recalling 2,000 pounds of Organic Yellow Peas sold between 10.17.2019 and 11.1.2020 because it may contain undeclared soybeans. People who have an allergy or severe sensitivity to soy run the risk of serious or life-threatening allergic reaction if they consume these products.
Maine Grains Organic Yellow Peas were distributed in the Northeastern United States and to online customers who ordered through mainegrains.comExternal Link Disclaimer. The majority of the product went to NYC.
No illnesses have been reported to date. Maine Grains is working with FDA officials on the recall.
The recall was initiated after it was discovered that organic soybeans of very similar size, shape and color to organic yellow peas were mistakenly shipped by a farmer supplier to Maine Grains, Inc. and were used to fulfill orders of organic yellow peas.
Retail bags are packaged in clear cellophane 1 lb bags and sold individually labelled as Maine Grains “Crop Rotation Organic Yellow Peas” bearing a lot number on a white sticker on the back of the bag ending in 3YP19. Customers may have purchased this product re-packaged under the GrowNYC brand label.
Maine Grains Organic Yellow Peas were also packed in 25 lb bulk bags labelled with Maine Grains, Inc., with contact information for the company in Skowhegan, ME and bearing a lot code on a small white sticker ending in 3YP19.
Consumers who have purchased Maine Grains Organic Yellow Peas between the dates of 10.17.2019 and 11.1.2020 are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1.207.474.8001, M-F 8-4 pm.

Bickel’s Snack Foods, Inc. Issues Allergy Alert on Specific Lot of Butter Flavored Popcorn

January 25, 2021

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Bickel’s Snack Foods, Inc. is voluntarily recalling one specific lot of 8 oz. Butter Flavored Popcorn bearing UPC code 70175 06021 due to the undeclared presence of milk. Consumers with an allergy or severe sensitivity to milk could experience a serious or life-threatening reaction if they consume this product.
The following Use By code is subject to this recall:
29 MAR 21
Z1 E1
No other products or lot codes are affected by this recall.
The product was sold to distributors in Georgia and North Carolina and is available exclusively in Publix Super Markets. The error occurred when bags containing Cheddar Flavored Popcorn were inadvertently labeled as Butter Flavored Popcorn. To date, there have been no illnesses reported in connection with the consumption of this product.
The error was identified by a store employee who alerted the manufacturer.
If you have this product in your possession, please discard it or return it to Publix for a full refund.
This voluntary recall is being made with the knowledge of the Food & Drug Administration.

House-Autry Mills Announces Voluntary Recall of House-Autry Tartar Sauce Due to Spoilage

January 22, 2021

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House-Autry Mills, Inc. is voluntarily recalling 9 oz. House-Autry Tartar Sauce (60013) with the following Best By dates: BB 08182021, BB 08232021, BB 09162021, BB 09172021, BB 09182021 and BB 09212021 as a precaution, due to the company’s co-manufacturer's verification of spoilage associated with the product. Several factors cause food spoilage, making items unsuitable for consumption. Light, oxygen, heat, humidity, temperature and spoilage bacteria can all affect both safety and quality of perishable foods. When subject to these factors, foods will gradually decline.
Samples have been issued to two separate laboratories for confirmation testing, but the company has decided to recall products produced from the specific lot received from the co-manufacturer to reduce any risk to our consumers.
The product was distributed between December 15, 2020 and January 18, 2021. The products are packaged in 9 oz. clear plastic bottles and sold to distribution centers in the following states: South Carolina, North Carolina, Virginia, Pennsylvania, Florida and Ohio.
No illnesses have been reported to date in connection with this issue.
The following products are affected by the recall:
Product Name: House-Autry Tartar Sauce – 9 oz. bottle
UPC: 0 73484-60013 4
BB 08182021 (located on the top portion of the bottle)
BB 08232021 (located on the top portion of the bottle)
BB 09162021 (located on the top portion of the bottle)
BB 09172021 (located on the top portion of the bottle)
BB 09182021 (located on the top portion of the bottle)
BB 09212021 (located on the top portion of the bottle)
Consumers who have purchased these products are urged to discontinue use and return them to the place of purchase for a full refund. Consumers with questions may contact the company by calling 1-800-849-0802, 8am-5pm EST daily, or by emailing Retail@House-Autry.com.

Publix Steam In Bag Product Recall

January 22, 2021

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Publix Super Markets, Inc. has initiated a voluntary recall on select Publix Steam In Bag products prepared in-store containing a specific butternut squash ingredient.
This recall is the result of notification of a recall for possible Listeria monocytogenes contamination from Pero Family Farms Company, LLC, the supplier of the butternut squash ingredient.
Pero Family Farms Food Company, LLC initiated a voluntary product recall of its Butternut Squash Trays because it has the potential to be contaminated with Listeria Monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
"As part of our commitment to food safety, potentially impacted product has been removed from all store shelves,” said Maria Brous, Publix communications director. "To date, there have been no reported cases of illness. Consumers who have purchased the products in question may return the product to their local store for a full refund. Publix customers with additional questions may call our Consumer Relations department at 1-800-242-1227 or visit our website at www.publix.comExternal Link Disclaimer.
Product Name    GTIN    Sold between
Publix Steam In Bag Green Bean Butternut Squash    002-24887-00000    01/03/2021-01/14/2021
Publix Steam In Bag Season Butternut Medley    002-25399-00000    01/03/2021-01/14/2021
Publix Steam In Bag Butternut Brussel Pecan    002-25677-00000    01/03/2021-01/14/2021

Frito-Lay Issues Voluntary Allergy Alert on Undeclared Milk in Small Number of Ruffles Original Potato Chip

January 22, 2021

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Frito-Lay today issued a voluntary recall of a small number of 13 1/2 oz. “Party Size” bags of Ruffles Original Potato Chips because they may contain undeclared milk ingredients. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume the product contained inside the recalled bags.  A total of 50 bags are being recalled.
The products covered by this recall were distributed to retail stores in Iowa, Kansas, Missouri, Nebraska, Oklahoma and Arkansas.
No other Ruffles products, sizes or flavors are recalled, including bags in Variety Packs.
The recall was initiated after it was discovered that 50 bags of Ruffles Original Potato Chips were inadvertently filled with another flavor of potato chips, potentially exposing consumers to undeclared milk.
No allergic reactions related to this matter have been reported to date. Frito-Lay has informed the FDA of the action.
Consumers with the product noted above can return the product to a retailer for a refund or contact Frito-Lay Consumer Relations at 1-800-352-4477 (9 a.m. – 4:30 p.m. CST, Monday-Friday).
The specific recalled product information is listed below:
Product Description    Size    UPC    Code Date/Price & Manufacturing Code    Representative Image
Ruffles
Original
Potato
Chips    13 1/2 oz.

PARTY SIZE    0 28400 03400 5    Both
“Guaranteed Fresh” date and price of 
23 MAR 2021
5.29

And
the Manufacturing Code
225335014
73  03:xx with xx = 00 through 13    See Product Image Below

Door County Coffee & Tea Co Issues Allergy Alert on Undeclared Milk and Soy in French Vanilla Flavored Cappuccino Single Serve Cups

January 22, 2021

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Door County Coffee & Tea Co of Sturgeon Bay, WI, is recalling its 5.1 ounce packages of French Vanilla Flavored Cappuccino Single Serve Cups because they may contain undeclared Milk and Soy. People who have allergies to Milk and Soy run the risk of serious or life-threatening allergic reaction if they consume these products.
The recalled French Vanilla Flavored Cappuccino Single Serve Cups were distributed in Wisconsin, Illinois, Iowa, Indiana, Kansas, Texas, Missouri, Florida and Michigan in grocery and gift stores and through mail orders.
The product comes in a 5.1 ounce full color cardboard box that contains 10 single sere cups, under the brand name Door County Coffee & Tea Co. The product was sold starting October 7th, 2020 with the lot code 1C092220-2 that expires 9/22/2022 and 1C120220-A that expires 12/2/2022.
No illnesses have been reported to date in connection with this problem.
The recall was initiated after it was discovered that product contains Milk and Soy was distributed in packaging that did not reveal the presence of these allergens. Subsequent investigation indicates the problem was caused by a printing omission.
Consumers who have purchased 5.1ounce packages of French Vanilla Flavored Cappuccino and are allergic to Milk and Soy are urged to discard the product and contact Door County Coffee & Tea Co for a refund. Consumers with questions may contact the company at 1-800-856-6613.

Bob Evans Farms Inc. Recalls Pork Sausage Product Due to Possible Foreign Matter Contamination

January 21, 2021

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– Bob Evans Farms, Inc. (“Bob Evans”), a Xenia, Ohio establishment, is recalling approximately 4,200 pounds of pork sausage product that may be contaminated with extraneous materials, specifically thin blue rubber, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The raw, pork sausage item was produced on December 17, 2020. The following products are subject to recall: [View Labels (PDF only)]
•    1-lb. chubs containing “Bob Evans Italian Sausage” with lot code 0352 and a “USE/FRZ BY” date of “JAN 31 21” represented on the label.
The products subject to recall bear establishment number “EST. 6785” printed directly above the “USE/FRZ BY” date. These items were shipped to retail locations in Indiana, Michigan, Ohio, Pennsylvania, and Wisconsin.
The problem was discovered when Bob Evans notified FSIS that they received consumer complaints.
Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers or both. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
Consumers and members of the media with questions about the recall can contact Alison Emery, Director of Communications, Bob Evans Farms Inc. at 614-778-1886 or alison.emery@bobevansfoods.com.

Lancaster Foods Recalls All Conventional Butternut Squash Items That Were Processed between the Dates of 12/22/20 and 01/08/21 Due to Possible Health Risk

January 20, 2021

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Lancaster Foods LLC has initiated a voluntary product recall of its processed butternut squash items because they have the potential to be contaminated with Listeria Monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
No illnesses have been reported to date in connection with this problem.
The recalled items were distributed in NC, VA, DC, MD, PN, NY, NJ, CT, RI, MA, NH, and VT mainly through retail stores.
The products noted:
1.    16 oz Autumn Medley - UPC 8 13055 01115 6; with the expiration dates of 01/05/21, 01/07/21, and 01/09/21 noted on the bottom scan label. The brand name is Lancaster Foods and the package is a clear plastic tamper-evident clamshell.
2.    12 oz Butternut Squash Noodles - UPC 8 13055 01749 3; with the expiration date of 01/10/21 noted on the bottom scan label. The brand name is Lancaster Foods and the package is a clear plastic tamperevident clamshell.
3.    12 oz Butternut Squash Noodles - UPC 8 13055 01864 3; with the expiration dates of 01/05/21, 01/08/21, 01/10/21, 01/11/21, 01/12/21, 01/15/21, and 01/17/21 noted on the bottom scan label. The brand name is Lancaster Foods and the package is a clear plastic tamper-evident clamshell.
4.    12 oz Butternut Squash Noodles - UPC 6 88267 17259 5; with the expiration dates of 01/08/21, 01/10/21, 01/12/21, 01/13/21, 01/14/21, 01/15/21, and 01/17/21 noted on the bottom scan label. The brand name is Store Brand and the package is a clear plastic tamper-evident clamshell.
5.    21 oz Butternut Squash Planks - UPC 8 13055 01272 6; with the expiration dates of 01/02/21, 01/08/21, 01/12/21, 01/15/21, and 01/17/21 noted on the bottom scan label. The brand name is Lancaster Foods and the package is a clear plastic tamper-evident clamshell.
6.    20 oz Squash Noodle Medley - UPC 8 13055 01836 0; with the expiration dates of 01/05/21, 01/08/21, 01/13/21, 01/14/21, and 01/16/21 noted on the bottom scan label. The brand name is Lancaster Foods and the package is a clear plastic tamper-evident clamshell.
7.    20 oz Squash Noodle Medley - UPC 6 88267 18585 4; with the expiration dates of 01/03/21, 01/08/21, 01/11/21, 01/17/21, 01/18/21, and 01/19/21 noted on the bottom scan label. The brand name is Store Brand and the package is a clear plastic tamper-evident clamshell.
8.    2.5# Butternut Squash Chunks - UPC 8 13055 01596 3; with the expiration dates of 01/04/21, 01/12/21, 01/15/21, and 01/18/21 noted on the bottom scan label. The brand name is Lancaster Foods and the package is a clear plastic tamper-evident clamshell.
9.    20 oz Butternut Squash Chunks - UPC 8 13055 01150 7; with the expiration dates of 01/05/21, 01/08/21, 01/09/21, 01/13/21, and 01/16/21 noted on the bottom scan label. The brand name is Lancaster Foods and the package is a clear plastic tamper-evident clamshell.
10.    24 oz Butternut Squash Chunks - UPC 8 13055 01300 6; with the expiration dates of 01/12/21, 01/13/21, 01/15/21 noted on the bottom scan label. The brand name is Lancaster Foods and the package is a clear plastic tamper-evident clamshell.
11.    12 oz Butternut Squash Chunks - UPC 8 13055 01391 4; with the expiration dates of 01/04/21, 01/05/21, 01/07/21, 01/11/21, 01/12/21, 01/15/21, 01/17/21, and 01/20/21 noted on the bottom scan labels. The brand name is Lancaster Foods and the package is a clear plastic tamper-evident clamshell.
12.    15 oz Veggie Rice Blend - UPC 8 13055 01014 2; with the expiration dates of 01/07/21 and 01/09/21 noted on the bottom scan labels. The brand name is Lancaster Foods and the package is a stand-up steam pouch with 'grab & steam' printed on the header.
Out of an abundance of caution, Lancaster Foods has temporarily halted production of these items as the FDA and the company investigate the source of the issue. Consumers who have purchased units noted above are urged to return them to the place of purchase for a full refund.
Consumers with questions may contact the company at 1-410-799-0010, extension 1530. The hours are from 0800 to 1700 in the Eastern time zone on the days of Monday through Sunday. Voicemails received after hours will be returned the next day.

Pero Family Farms Food Co. Issues Voluntary Recall Due to Possible Health Risk

January 20, 2021

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Pero Family Farms Food Company, LLC has initiated a voluntary product recall of its Butternut Squash Trays because it has the potential to be contaminated with Listeria Monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. Below is a product listing of the affected butternut products:
Run No.    Item's Name:    USE BY DATE
1222496F    12oz Pero Family Farms Veggie Butternut Squash Tray    1/15/2021
1222496F    10oz Pero Family Farms Butternut Spirals Tray    1/15/2021
1222496F    13oz Pero Family Farms Cubed Butternut Tray    1/13/2021
1222496F    9.5oz Pero Family Farms Butternut Veggie Spirals Tray    1/13/2021
1222496F    4/5lbs Butternut Chunk Bag    1/13/2021
1222496F    2/5lbs Butternut Chunk Bag    1/13/2021
Run No.    Item's Name:    USE BY DATE
1222747F    Pero Family Farms 12oz Prep Veggie Butternut Squash Tray    1/16/2021
1222747F    Pero Family Farms 10oz Butternut Spirals Tray    1/16/2021
1222747F    Pero Family Farms 13oz Cubed Butternut Tray    1/14/2021
1222747F    Pero Family Farms 9.5oz Butternut Veggie Spirals Tray    1/14/2021
Run No.    Item's Name:    USE BY DATE
1222831F    Pero Family Farms 10oz Butternut Spirals Tray    1/17/2021
1222831F    Pero Family Farms 13oz Cubed Butternut Tray    1/15/2021
1222831F    Pero Family Farms 9.5oz Butternut Spirals Tray    1/15/2021
1222831F    Pero Family Farms 5lb Butternut Chunk Bag    1/15/2021
Run No.    Item's Name:    USE BY DATE
1222851F    Pero Family Farms 10oz Butternut Spirals Tray    1/18/2021
1222851F    Pero Family Farms 13oz Cubed Butternut Tray    1/16/2021
1222851F    Pero Family Farms 9.5oz Butternut Spirals Tray    1/16/2021
Run No.    Item's Name:    USE BY DATE
1222959F    Pero Family Farms 12oz Prep Veggie Butternut Squash Tray    1/19/2021
1222959F    Pero Family Farms 10oz Butternut Spirals Tray    1/19/2021
1222959F    Pero Family Farms 13oz Cubed Butternut Tray    1/17/2021
1222959F    Pero Family Farms 9.5oz Butternut Spirals Tray    1/17/2021
Run No.    Item's Name:    USE BY DATE
1223108F    Pero Family Farms 10oz Butternut Spirals Tray    1/20/2021
1223108F    Pero Family Farms 13oz Cubed Butternut Tray    1/18/2021
1223108F    Pero Family Farms 9.5oz Butternut Spirals Tray    1/18/2021
1223108F    Pero Family Farms 5lb Butternut Chunk Bag    1/18/2021
Run No.    Item's Name:    USE BY DATE
1223145F    Pero Family Farms 10oz Butternut Spirals Tray    1/21/2021
1223145F    Pero Family Farms 13oz Cubed Butternut Tray    1/19/2021
1223145F    Pero Family Farms 9.5oz Butternut Spirals Tray    1/19/2021
Run No.    Item's Name:    USE BY DATE
1223223F    Pero Family Farms 12oz Veggie Butternut Squash Tray    1/22/2021
1223223F    Pero Family Farms 10oz Butternut Spirals Tray    1/22/2021
1223223F    Pero Family Farms 13oz Cubed Butternut Tray    1/20/2021
1223223F    Pero Family Farms 9.5oz Butternut Spirals Tray    1/20/2021
1223198F    Pero Family Farms 5lb Butternut Chunk Bag    1/20/2021
This product was processed by Pero Family Farms Food Company, LLC and distributed under the Pero Family Farms Label in Louisiana, Florida, Texas, New York, Maine, Georgia, Ohio, Virginia, Alabama, Virginia and Missouri. It is packaged in a flexible clear plastic containers with labeling on the top and bottom of the container or in a clear plastic bag. The product run number code and use by date can be found on the front bottom right hand corner of the tray package or on the package. These items were distributed from January 2, 2021- January 11, 2021 and were distributed to wholesalers and retail food stores.
No illnesses have been reported to date in connection with this issue. This voluntary recall was the result of notification of possible Listeria contamination from Race West Company, a supplier of butternut squash to Pero Family Farms. Pero Family Farms Food Company, LLC has temporarily halted production of these items as all parties continue their investigation into this issue. Consumers who may have purchased this product are urged to return the product back to the place of purchase for a full refund or discard this product.
 

Hiland Dairy Announces Recall of Hiland Dairy Half-Pint 1% Low Fat Chocolate Milk Cartons

January 19, 2021

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Hiland Dairy is announcing a recall of the one-half pint (236 mL) 1% low fat chocolate milk that was produced at its Norman, Oklahoma facility only. Some of the products may contain food-grade sanitizers, which could cause illness if consumed.
The affected products were sold and distributed to institutional customers in the following areas:
•    Oklahoma City, Oklahoma Metro Area
•    Western Oklahoma
•    Dallas, Texas
•    San Antonio, Texas
•    Tyler, Texas
The product information is detailed below:
One-Half Pint Hiland Dairy 1% Low Fat Chocolate Milk
UPC: 72060-00156-3
Sell by Date: January 27, 2021
Plant Code: 4025
1% Lowfat Chocolate Milk Half Pint
Affected Code Date: 1/27/21 (See Image Below)
ONLY Products with plant code #4025 are included. (See Image Below)
Hiland Dairy initially learned of a potential issue and then confirmed after internal quality-control testing at the Norman, Oklahoma facility. The company promptly contacted the U.S. Food and Drug Administration (FDA) to initiate the product recall.
To ensure 100% containment, Hiland Dairy is recalling all of the product with 1/27 code, although there were only eight cases affected. There are 50 units of one-half pints in one case and 4,800 cases were distributed with the above codes for a total of 240,000 units of one-half pint Hiland 1% Low Fat Chocolate Milk.
Other Hiland Dairy products are not part of this recall.
Hiland Dairy is working in partnership with the FDA to fully investigate the matter and comply with all necessary recall procedures.
Consumers with questions may contact Hiland Dairy seven days a week from 8 a.m. to 5 p.m. CST via email at https://www.hilanddairy.com/contact-usExternal Link Disclaimer.

Potential Foreign Object Recall Lake Champlain Chocolates Issues Voluntary Recall on Selected Milk Chocolate Products

January 19, 2021

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Lake Champlain Chocolates (LCC) is issuing a public alert and a voluntary recall on select LCC milk chocolate products from a determined best-by date range for potential foreign objects. LCC is issuing this recall after a consumer reported finding brittle plastic pieces in a finished product. After initial investigations and out of an abundance of caution, LCC is voluntarily recalling all potential affected product currently on the market from July 2020 through January 2021. To date, no consumers have reported adverse health effects due to this contamination.
Affected products include:
•    HazelnutExternal Link Disclaimer Five Star Bar
•    Fruit & NutExternal Link Disclaimer Five Star Bar
•    AlmondExternal Link Disclaimer Five Star Bar
•    GranolaExternal Link Disclaimer Five Star Bar
•    Organic Milk Chocolate Bar with Sea Salt & AlmondsExternal Link Disclaimer
•    Milk Chocolate Almond Bark
•    Chocolates of Vermont Green MountainExternal Link Disclaimer
 These products can be found within a variety of other gift packages, boxes and baskets.  Please refer to the document at the end of this release for a detailed list of all affected products and associated Best By Dates.
These products were distributed through retailers and distributors across all fifty states and in the company’s three Vermont retail stores.
The FDA has been informed of this voluntary recall and will post this notice on their website.
LCC is asking customers to discontinue use and immediately dispose of any products listed above. Customers can find the Best By Date near the UPC code on the package. For any additional questions or concerns please email  info@lakechamplainchocolates.com.
Lake Champlain Chocolates is committed to quality products and consumer safety and is taking aggressive corrective action to prevent the need for any future recalls of its products.  It emphasizes that no other LCC products or batch codes were affected.
Lake Champlain Chocolates apologizes for any inconvenience to its consumers and customers.
List of Items and Best By Dates Affected:
Stock Code    Item Description    UPC    LOT#    Best by
1V301-015001-1    GALENTINE SELECTION 15PC BOX 9oz    76993385787    20343    3/8/2021
               20356    3/21/2021
               21004    4/4/2021
               21011    4/11/2021
1V315-000001-1    BASKET BE MINE Net Wt. 2lbs    76993305237    21004    4/4/2021
1X301-015001-1    HOLIDAY SELECTION 15PC BOX 9oz    76993304604    20303    1/27/2021
               20309    2/2/2021
               20316    2/9/2021
               20330    2/23/2021
               20342    3/7/2021
               20351    3/16/2021
               20356    3/21/2021
1X301-030001-1    HOLIDAY SELECTION 30PC BOX 1.1 lbs    76993304605    20301    1/25/2021
               20311    2/4/2021
               20329    2/22/2021
               20335    2/28/2021
               20345    3/10/2021
1X302-016001-1    HOLIDAY CHOCOLATES OF VERMONT 16PC BOX 7.6oz    76993385319    20269    2/22/2021
               20280    2/3/2021
               20288    2/11/2021
               20295    2/18/2021
               20308    3/3/2021
               20311    3/6/2021
               20323    3/18/2021
               20325    3/20/2021
               20349    4/13/2021
               20352    4/16/2021
               20357    4/21/2021
1X315-000002-1    BASKET OF CHEER 2.4lbs    76993305235    20289    1/13/2021
               20307    1/31/2021
               20321    2/14/2021
               20338    3/3/2021
1X315-000003-1    TIS THE SEASON GIFT BASKET 1.5lbs    76993385408    20289    3/14/2021
               20307    4/1/2021
               20322    4/16/2021
               20339    5/3/2021
1Y301-030002-1    SELECTION ASST 30PC BOX1.1lbs    76993304603    20301    1/25/2021
               20311    2/4/2021
               20328    2/21/2021
               20342    3/7/2021
1Y301-015001-1    SELECTION ASST 15PC BOX 9oz    76993304602    20303    1/27/2021
               20316    2/9/2021
               20321    2/14/2021
               20329    2/22/2021
               20345    3/10/2021
               21011    4/11/2021
1Y302-000000-1    CHOCOLATES OF VERMONT ASST BULK 2.5lbs    76993305399    20267    2/20/2021
               20280    2/3/2021
               20287    2/10/2021
               20303    2/23/2021
               20321    3/16/2021
               20339    4/3/2021
               20351    4/15/2021
               20365    4/29/2021
               21012    5/12/2021
1Y302-004001-1    CHOCOLATES OF VERMONT 4PC SAMPLER 1.9oz    76993302007    20259    1/12/2021
               20268    1/21/2021
               20289    2/12/2021
               20304    2/24/2021
               20315    3/10/2021
               20323    3/18/2021
               20356    4/20/2021
               21008    5/8/2021
1Y302-008001-1    CHOCOLATES OF VERMONT ASST 8PC BOX 3.8oz    76993302010    20260    2/13/2021
               20269    2/22/2021
               20294    2/17/2021
               20310    3/5/2021
               20325    3/20/2021
               20339    4/3/2021
               20357    4/21/2021
               21012    5/12/2021
1Y302-012001-1    CHOCOLATES OF VERMONT ASST 12PC BAG 5.7oz    76993385322    20260    2/13/2021
               20269    2/22/2021
               20295    2/18/2021
               20309    3/4/2021
               20323    3/18/2021
               20345    4/9/2021
               20365    4/29/2021
               21012    5/12/2021
1Y302-024002-1    CHOCOLATES OF VERMONT ASST 24PC BOX 11.4oz    76993385454    20273    2/26/2021
               20295    2/18/2021
               20314    3/9/2021
               20324    3/19/2021
               20349    4/13/2021
               21006    5/6/2021
1F302-016001-1    CHOCOLATES OF VERMONT FALL 16PC BOX 7.6OZ    76993385374    20308    3/3/2021
               20293    2/16/2021
               20269    1/23/2021
                     
1Y302-085004-1    CHOCOLATES OF VERMONT GREEN MOUNTAIN MK BK 2.5lbs    76993302005    20273    3/28/2021
               20308    5/2/2021
               20329    5/23/2021
               20357    6/20/2021
1Y304-006002-1    FIVE STAR BAR 6 PACK ASST*FT 11.4oz    76993385688    20231    2/14/2021
               20274    3/29/2021
               20286    4/10/2021
               20309    5/3/2021
               20315    5/9/2021
               20324    5/18/2021
               20343    6/6/2021
               20349    6/12/2021
               20352    6/15/2021
               20353    6/16/2021
               20356    6/19/2021
               20363    6/26/2021
               21006    7/5/2021
1Y310-000017-1    ALMOND BARK MK BK    76993303050    20310    1/15/2021
1Y315-000001-1    THE CHOCOLATE TOWER 2.2lbs    76993305230    20296    1/20/2021
               20303    1/27/2021
               20335    2/28/2021
               20350    3/15/2021
               20358    3/23/2021
               20363    3/28/2021
               21011    4/11/2021
1Y315-000002-1    DARK CHOCOLATE GIFT BASKET 2.6lbs    76993305231    20308    3/3/2021
               20317    3/12/2021
               20329    4/3/2021
               20349    4/13/2021
               20353    4/15/2021
1Y315-000005-1    SIGNATURE GIFT BASKET 2.8lbs    76993305232    20296    1/20/2021
               20300    1/24/2021
               20304    1/28/2021
               20317    2/10/2021
               20321    2/14/2021
               20342    3/7/2021
               20351    3/16/2021
               20363    3/28/2021
1Y315-000006-1    VT COUNTRY GIFT BASKET 1.2lbs    76993305233    20261    2/14/2021
               20268    1/22/2021
               20281    2/4/2021
               20293    2/16/2021
               20301    2/21/2021
               20309    3/4/2021
               20329    4/3/2021
               20344    4/8/2021
1Y304-024002-1    FIVE STAR BAR FRUIT&NUT DK*FT 1.9oz    76993300502    20217    1/31/2021
               20254    3/9/2021
               20273    3/28/2021
               20290    4/14/2021
               20289    4/13/2021
               20314    5/8/2021
               20335    5/29/2021
               20353    6/16/2021
               21008    7/7/2021
               21011    7/10/2021
1Y304-024004-1    FIVE STAR HAZELNUT BAR MK*FT 1.8oz    76993300504    20204    1/18/2021
               20209    1/23/2021
               20212    1/26/2021
               20213    1/27/2021
               20225    2/8/2021
               20231    2/14/2021
               20227    2/10/2021
               20238    2/21/2021
               20241    2/24/2021
               20245    2/28/2021
               20254    3/9/2021
               20266    3/21/2021
               20267    3/22/2021
               20275    3/30/2021
               20286    4/10/2021
               20294    4/18/2021
               20288    4/12/2021
               20290    4/14/2021
               20303    4/27/2021
               20308    5/2/2021
               20311    5/5/2021
               20307    5/1/2021
               20317    5/11/2021
               20321    5/15/2021
               20328    5/22/2021
               20335    5/29/2021
               20329    5/23/2021
               20336    5/30/2021
               20344    6/7/2021
               20346    6/9/2021
               20353    6/16/2021
               20357    6/20/2021
               20358    6/21/2021
               20365    6/28/2021
               21006    7/5/2021
               21008    7/7/2021
1Y304-024005-1    FIVE STAR BAR GRANOLA DK*FT 1.9oz    76993385318    20209    1/23/2021
               20240    2/23/2021
               20275    3/30/2021
               20308    5/2/2021
               20335    5/29/2021
               21006    7/5/2021
1Y304-024008-1    FIVE STAR ALMOND DK*FT 1.85oz    76993385800    20204    1/18/2021
               20217    1/31/2021
               20241    2/24/2021
               20276    3/31/2021
               20309    5/3/2021
               20336    5/30/2021
               21005    7/4/2021
1Y504-012105-1    ALMOND SEA SALT BAR 43%MK ORG 3oz    76993385498    20284    7/7/2021
1Y515-000001-1    MILK CHOCOLATE BAR LIBRARY ORG 1.1lbs    76993385757    20321    3/24/2021
               20323    4/2/2021
               20342    5/8/2021
1Y515-000004-1    CLASSIC BAR LIBRARY ORG 1.1lbs    76993385760    20349    5/8/2021

FSIS Issues Public Health Alert for Beef Jerky Products Due to Misbranding and an Undeclared Allergen

January 19, 2021

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The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) beef jerky products due to misbranding and an undeclared allergen. The product may contain anchovies, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert out of the utmost of caution to ensure that consumers with allergic reactions to anchovies are aware that these products should not be consumed. This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product because of the presence in a product of very small amounts of the undeclared allergens are typically associated with milder human reactions. A recall was not requested because the products are not currently available for sale to consumers.
The RTE beef jerky products were produced from October 20, 2020 through January 12, 2021 and have a one-year shelf life. The product labeled as “CHARLIE BROWN FARMS PREMIUM BEEF JERKY Original Prime Rib” contains Worcestershire, which is not listed as an ingredient, but was utilized in the product formulation. The following products are subject to the public health alert: [View Labels (PDF only)]
•    3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY PEPPERED BEEF”
•    3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY OLD FASHIONED”
•    4-oz. gold foil bags of “SETTLERS JERKY HOT BEEF”
•    3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY PRIME RIB”
•    3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY RING OF FIRE BEEF JERKY”
•    3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY GHOST PEPPER”
•    3.25-oz. silver bags of “Sierra Madre Provision Co. OLD FASHIONED BEEF JERKY”
•    3.25-oz. silver bags of “Sierra Madre Provision Co. PEPPERED BEEF JERKY”
•    3.25-oz. silver bags of “Sierra Madre Provision Co. HOT BEEF JERKY”
•    3.25-oz. silver bags of “Sierra Madre Provision Co. GHOST PEPPER BEEF JERKY”
•    3.25-oz. silver bags of “Sierra Madre Provision Co. RING OF FIRE BEEF JERKY”
•    3-oz., 4-oz. and 8-oz. silver bags of “CHARLIE BROWN FARMS PREMIUM FRESH BEEF JERKY GHOST PEPPER”
•    3-oz. and 4-oz. gold bags of “CHARLIE BROWN FARMS PREMIUM FRESH BEEF JERKY Original Prime Rib”
•    3-oz. and 4-oz. gold bags of “CHARLIE BROWN FARMS PREMIUM FRESH BEEF JERKY RING OF FIRE”
The products bear establishment number “EST. 8275” inside the USDA mark of inspection. These items were distributed for wholesale and also sent to retail locations in California.
FSIS is concerned that some product may be in consumers’ pantries.
The problem was discovered by FSIS inspection personnel. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumers with food allergies who have purchased these products are urged not to consume them. These products should be thrown away.

Lavva Voluntarily Recalls a Single Lot of Blueberry Plant-Based Yogurt

January 11, 2021

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Out of an abundance of caution, EVR Foods, INC, parent company to Lavva, is issuing a voluntary recall on its 5.3 ounce Blueberry Plant-Based Yogurt with expiration date 2/21/21. While this SKU and date code cleared strict quality assurance protocols, recent testing indicates a potential mold contamination. No other Lavva products are affected by the recall.
This plant-based yogurt was produced at a manufacturing facility in Norwich, NY, and has only been linked to the single date code. There have been no confirmed illnesses to date.
The recalled Blueberry Plant-Based Yogurts were distributed to retail stores nationwide. The product comes in a 5.3 ounce, colorful plastic cup with a foil lid, marked with lot #022121 on the bottom of the cup which is also used as the expiration date of the product.
Consumers are urged not to eat the product subject to the recall. Anyone who purchased the SKU may return it to the place of purchase for a full refund. Consumers with questions about the recall can reach out to hello@lovvelavva.com or 833-885-2882 between 9 a.m. to 5 p.m. EST Monday through Friday. The Food & Drug Administration (FDA) has been notified of this recall and is assisting with the process.

Essaar Inc. Issues Voluntary Nationwide Recall of Rubbing Alcohol Contaminated with Methanol

January 4, 2021

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Essaar Inc. is voluntarily recalling lot 200528303 of Soho Fresh 70% Rubbing Alcohol in 33.81 oz. clear plastic bottles to the consumer level. FDA analysis of the product revealed it is contaminated with methanol.
Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, Essar Inc. has not received any reports of adverse events related to this recall.
The product is used as an external purpose use rubbing alcohol and is packaged in 33.81 oz. clear plastic bottles with lot number 200528303 and UPC 7502268987367.
Soho Fresh was distributed nationwide to retail stores. Essaar Inc. is notifying its distributors and customers by email and mail and is arranging for the return of all recalled product to Essaar Inc. Consumers that have product which is being recalled should stop using and discard or return to place of purchase or to Essaar Inc. contacting via email or phone or mailing address mentioned above for arrangements of return.
Consumers who have purchased this product should not open the package or use the contents. Instead, they should return the product to the location of purchase for a full refund or call Essaar Inc. at 201-647-7606 Monday to Friday 9am to 5pm, Eastern Standard Time. Essaar Inc. can also be reached via email at essaarinc@yahoo.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Dole Fresh Vegetables Announces Limited Voluntary Recall of Dole™ Sesame Asian Chopped Salad Kit Due to Undeclared Allergens

January 5, 2021

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Dole Fresh Vegetables, Inc. is voluntarily recalling a limited number of cases of Dole™ Sesame Asian Chopped Salad Kit.
Description    UPC    Best If Used By Date    Lot Code
Dole™ Sesame Asian Chopped Salad    0-71430-00035-9    01-15-21    B364016
B364017
This voluntary recall is due to possible undeclared allergens (egg) in Dole™ Sesame Asian Chopped Salad Kit. The dressing and topping kit (masterpack) designed for a different Dole product was unintentionally used during a portion of the production of the salad. Dole Fresh Vegetables, Inc. is coordinating closely with regulatory officials. No illnesses or allergic reactions have been reported to date in association with the recall. However, people who have an allergy to eggs may have a serious or life-threatening allergic reaction if they consume this product or products containing eggs.
p> The product lot code and Best if Used by Date is located on the upper right corner of each bag and the UPC code is located on the bottom right corner of the back of each bag. The impacted products were distributed in AK, CA, ID, KS, MO, OK, OR, TX AND UT. Consumers are advised to check product they have in their homes and discard any product matching the production description, UPC codes, product lot code and Best if Used by Date listed above.
No other Dole products are included in the recall. Only Dole™ Sesame Asian Chopped Salad Kit with the exact UPC code, lot code and Best if Used by Date identified above, are included in the recall. Consumers who have any remaining product should not consume it, but rather discard it. Retailers and consumers with questions may call the Dole Consumer Center at 1-800-356-3111, which is open 24 hours a day.

Weis Markets Issues Recall for Possible Foreign Matter Contamination in Weis Ice Cream Products

January 8, 2021

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Weis Markets today said it has issued a recall for:
•    10,869 containers of Weis Quality Cookies and Cream Ice Cream (48 oz.), and
•    502 bulk containers of Klein’s Vanilla Dairy Ice Cream (3 gallon)
because the products may be contaminated with extraneous material, specifically metal filling equipment parts. There has been one report of a customer who discovered an intact piece of metal equipment in the Weis Quality Cookies and Cream Ice Cream (48 oz). There is concern of an additional piece of equipment present in the ice cream product(s) possibly presenting a choking hazard.
The Weis Quality Cookies and Cream Ice Cream (in 48 oz. containers) product has been removed from sale. It was sold in 197 Weis Markets’ stores in Pennsylvania, Maryland, Virginia, New Jersey, New York, Delaware and West Virginia.
The Weis Quality Cookies and Cream ice cream is packaged in a scround 48- ounce container with a UPC of 041497-01253 and with a sell by date of 10/28/21. This was produced on 10/28/2020 and released for sale on 10/29/2020. The sell by date is located on the bottom of the container. An example of the label has been included with this release. Customers who have purchased this product may return it for a full refund.
The Klein’s Vanilla bulk ice cream is packaged in 3-gallon containers with a code stamp of 0302 and are not for retail sale. This product was sold to one retail establishment in New York and has been removed from sale.
Additional ice cream products packaged on 10/28/2020 included:
•    Klein’s Cookies and Cream Dairy Bulk – 665 containers, and
•    Nelson’s Graham Slam Bulk – 286 containers
These items are packaged in 3-gallon bulk containers with a code stamp of 0302 and are not for retail sale. They were stored in a warehouse and have not been distributed.
Customers requiring additional information may contact Weis Customer Service at 1-866-999-9347 Monday through Friday 8am-5pm EST.

FSIS Issues Public Health Alert for Not-Ready-to-Eat, Heat Treated, Not Fully Cooked Chicken Enchilada Products Due to Misbranding and an Undeclared Allergen

January 7, 2021

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The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for approximately 43 pounds of not-ready-to-eat (NRTE), heat treated, not fully cooked chicken enchilada products due to misbranding and an undeclared allergen. FSIS is issuing this public health alert out of the utmost of caution to ensure that consumers with allergic reactions to soy are aware that these products should not be consumed. A recall was not requested because the chicken enchilada products are no longer available in commerce.
The NRTE product labeled as “HyVee mealtime CHICKEN ENCHILADAS” was produced on Jan. 3, 2021. The following product is subject to the public health alert: [View Label (PDF only)]
•    62.4-oz. (3-lbs. 14.4-oz.) heat and serve container of “HyVee mealtime CHICKEN ENCHILADAS” with lot code “21003” and “Best If Use By: 01/10/2021” date on the product label.
The products bear establishment number “P51558” inside the USDA mark of inspection. These items were distributed to HyVee retail locations in Illinois, Iowa, Kansas, Minnesota, Missouri, Nebraska, South Dakota and Wisconsin.
The problem was discovered when a HyVee retail store employee identified the labeling issue and reported it to the establishment.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers with food allergies who have purchased these products are urged not to consume them. These products should be thrown away.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.

Courage Production, LLC. Recalls Ready-to-Eat, Fully Cooked Polish Sausage Products due to Misbranding and an Undeclared Allergen

January 3, 2021

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WASHINGTON, Jan. 2, 2021 – Courage Production, LLC., a Fairfield, Calif., establishment is recalling approximately 1,645 pounds of Ready-To-Eat, fully cooked Polish sausage products due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products contain milk (mozzarella cheese), a known allergen that is not declared on the product label. 
The sausage products labeled as “TETON WATERS RANCH POLISH SAUSAGE,” may contain a sausage product with mozzarella cheese. The products were produced on Oct. 9, 2020. The following products are subject to recall [View Labels (PDF Only)]:
•    10-oz. vacuum packed packages of four “TETON WATERS RANCH POLISH SAUSAGE” with lot code “202831,” “Use or Freeze By: JAN/8/21” date and bear  establishment number “Est. 6024” on the side of the packaging label.
These items were shipped to retail locations in California, Colorado, Indiana, Maryland, Maine, New York and Oregon.                      
The problem was discovered after the firm received notification of a customer complaint that product labeled as “Teton Waters Ranch Polish Sausage,” contained red bell peppers, as well as mozzarella cheese, which were not included on the product label.  
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.   
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased this product are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers with questions about the recall can contact Shane Osterthaler, Director of Food Safety at Courage Production, LLC., at (707) 422-6300. Members of the media with questions about the recall can contact Rob Engelhart, President of Courage Production, LLC., at (707) 422-6300.

FSIS Issues Public Health Alert for Frozen, Fully Cooked, Not Shelf Stable Chicken Sriracha Ravioli Products Due to Misbranding and an Undeclared Allergen

January 3, 2021

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WASHINGTON, Dec. 31, 2020 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for approximately 49 pounds of frozen, fully cooked, not shelf stable chicken sriracha ravioli products due to misbranding and an undeclared allergen. The product may contain soy, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert out of the utmost of caution to ensure that consumers with allergic reactions to soy are aware that these products should not be consumed. A recall was not requested because it is believed that the affected products are no longer available to be directly purchased by consumers in retail.
The product labeled as “FRESH THYME FARMERS MARKET CHICKEN RAVIOLI Ovals” was formulated with a different sriracha chili sauce than normally utilized in the product formulation because the firm was unable to obtain the usual brand from their supplier. The sriracha chili sauce used on Dec. 8, 2020 contains soy, while the sauce normally used in the formulation does not. The following products are subject to the public health alert: [View Labels (PDF only)]
•    16-oz. plastic bags of “FRESH THYME FARMERS MARKET CHICKEN RAVIOLI Ovals” with best-by date “12/08/2021.”
The products bear establishment number “EST. M-1854/P-19980” inside the USDA mark of inspection. These items were shipped to distributors/sold in retail in Illinois, Indiana, Kentucky, Michigan, Minnesota, Missouri, Ohio, Pennsylvania and Wisconsin.
FSIS is concerned that some product may be in consumers’ freezers.
The firm’s Quality Assurance Director discovered the problem during a label review. There is no product currently available for sale to consumers. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumers with food allergies who have purchased these products are urged not to consume them. These products should be thrown away.

Lipari Foods Issues Allergy Alert on Undeclared Milk in Backroad Country Spicy Cajun Mix

December 31, 2020

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Lipari Foods of Warren, MI is recalling its 9 ounce packages of Backroad Country Spicy Cajun Mix because it contains undeclared milk. People who have allergies to milk run the risk of serious or life-threatening allergic reaction if they consume these products.
The recalled Backroad Country Spicy Cajun Mix were distributed nationwide in retail stores.
The product comes in a 9 ounce, clear plastic package marked with lot #M24501, M26902 with an expiration of 11/2021 on the back of the package and M28201 with an expiration of 12/2021 on the back of the package.
No illnesses have been reported to date in connection with this problem.
The recall was initiated after it was discovered that the milk-containing product was distributed in packaging that did not reveal the presence of milk. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's production and packaging processes.
Production of the product has been suspended until FDA and the company are certain that the problem has been corrected.
Consumers who have purchased 9 ounce packages of Backroad Country Spicy Cajun Mix are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Lipari Foods at 1-586-447-3500. Normal business hours are Monday through Friday 9:00am to 5:00pm.

Divvies, LLC Issues Allergy Alert on Undeclared Milk and Eggs in Vanilla Cupcakes

December 31, 2020

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Divvies of Trumbull, CT is recalling Vanilla Cupcakes with Vanilla Frosting and Vanilla Cupcakes with Chocolate Frosting because they may contain undeclared milk and eggs.
People who have an allergy or severe sensitivity to milk or eggs run the risk of serious or life-threatening allergic reaction if they consume these products.
Product was distributed nationwide in retail stores and online websites. This distribution was limited to 472 cases in total.
The product comes in a 6-ounce, clear plastic clamshell labelled with the Divvies brand and marked with a lot # VV303-1, VV304-1, or VC309-1 on the side of the container.
No illnesses have been reported to date in connection with this problem.
The recall was initiated after it was discovered that an ingredient containing milk and eggs had gotten into the ingredient mix which is used specifically for the vanilla cupcakes. This happened when the mix was packaged by the ingredient supplier.  Subsequent investigation indicates the problem was caused by a temporary breakdown of a piece of equipment on the supplier’s packaging line.  The problem has been corrected.
Consumers who have purchased the 6oz package of Divvies Vanilla Cupcakes with Vanilla Frosting or Divvies Vanilla Cupcakes with Chocolate Frosting with Lot #’s VV303-1, VV304-1, or VC309-1 are urged to return the product to the place of purchase for a full refund.
Consumers with questions may contact the company at 203-989-3173.

FSIS Issues Public Health Alert for Ineligible Imported Raw Frozen New Orleans - Roasted Chicken Wings from the Peoples Republic of China

December 21, 2020

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WASHINGTON, Dec. 19, 2020 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for raw frozen New Orleans -Roasted Chicken Wings products imported and labeled with a false USDA mark of inspection. A recall was not requested because the known affected product is no longer available in commerce for consumers to purchase.  
Di-Da Di-Da USA Corp., a Saratoga, Cal., establishment received and distributed ineligible imported frozen chicken wings products from The Peoples Republic of China to U.S. commerce for retail sale.
The following product is subject to the public health alert: [View Labels (PDF only)]
•    600 gram bags of “Chicken Arrived, Organic Chicken, NEW ORLEANS- ROASTED CHICKEN WINGS”, with “Best before” date of 09/19/2021 written in mandarin language.
The products were shipped to one retail location and then further distributed to 20 different retail locations in California, Oregon, and Washington. The frozen chicken wings products are labeled with a false USDA mark of inspection bearing “P-40478”, an establishment number that does not exist.
The problem was discovered when FSIS received a consumer complaint reporting a product suspected of being illegally imported being sold at a location. After investigation, FSIS determined that the product was ineligible and misbranded with a false USDA mark of inspection. 
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.  
FSIS is concerned that some product may be in consumers’ freezers. Retailers who have purchased the product are urged not to sell it. Consumers who purchased the product should not consume it and properly discard it. Consumers are asked to double bag the product when discarding it to reduce the possibility of animals accessing the product because USDA cannot confirm whether the chicken wings were properly heated to control pathogens of concern to domestic livestock.

O&H Danish Bakery, Inc. Issues Allergy Alert on Potential for Undeclared Pecans in Almond Kringle

December 19, 2020

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O&H Danish Bakery, Inc. of Racine, WI is recalling 3,173 units of Almond Kringle (1lb 8oz) with batch code 26720 sold in Trader Joe’s retail stores because it may contain undeclared Pecans. People who have allergies to pecans run the risk of serious or life-threatening allergic reaction if they consume these products.
The recalled Almond Kringle were delivered to the Trader Joe’s stores located in Texas, Tennessee, Oklahoma, New Mexico, Louisiana, Colorado, Kansas, Arkansas and Alabama.
The product is packaged in a white wax paper bakery bag marked with batch code #26720. The batch code can be found in the upper right-hand corner of the product nutritional label (see diagram referenced below).
No illnesses have been reported to date in connection with this problem.
The recall was initiated because it was discovered that four pecan filled kringles were incorrectly labeled as Almond Kringle and delivered to the Trader Joe’s distribution center as a part of a larger order. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's baking and icing processes.
People who have an allergy to pecans run the risk of serious or life-threatening allergic reaction if they eat this product. If you purchased the Almond Kringle with the specified batch code from a Trader Joe’s store in one of the nine states listed and have a pecan allergy, please do not eat it. We urge you to discard the product or return it to any Trader Joe’s for a full refund. Alternatively, you may send an email to TJrecall@ohdanishbakery.com with a picture of the product label for a replacement item delivered to your door.
Should you have any additional questions or concerns we urge you to please contact our president, Eric Olesen, at 262-631-5398 to discuss further.

Perfect Pasta Inc. Recalls Frozen Meat and Poultry Products Produced Without Benefit of Inspection

December 19, 2020

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WASHINGTON, Dec. 19, 2020 - Perfect Pasta Inc., an Addison, Ill. establishment, is recalling an undetermined amount of heat treated not shelf stable frozen meat and poultry products that were produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The various packages of frozen meat and poultry products were produced between December 2018 and December 2020 and bear an establishment number “Est. 19829/P-19829” inside the USDA mark of inspection.
All products subject to the recall can be found on the following [Recall Products List (PDF only)]. These items were distributed and sold nationwide.
The problem was discovered when an FSIS investigation determined the firm was reportioning and repackaging amenable products in a secondary location without the benefit of federal inspection. The repackaging facility does operate under the USDA Grant of Inspection for Est.19829/P-19829.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.  
FSIS is concerned that some product may be frozen and in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Quality Assurance Director, Connie DeMarco and Quality Assurance Manager, Paul Novak at (630) 543-8300.

FSIS Issues Public Health Alert for Ready-to-Eat Pork Snack Stick Products Due to Misbranding and an Undeclared Allergen

December 17, 2020

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WASHINGTON, Dec. 17, 2020 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) pork snack stick products due to misbranding and an undeclared allergen. The product may contain milk, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert out of the utmost of caution to ensure that consumers with allergic reactions to dairy are aware that these products should not be consumed. A recall was not requested because the pork products were sold directly to individual members of the public and it is believed that the affected products are no longer available to be directly purchased from the establishment.
The RTE product labeled as “Country Meats HOT BBQ Flavor Smoked Pork Snack Sticks” may actually contain Chili Cheese flavor pork snack sticks and was produced on November 6, 2020. The following products are subject to the public health alert: [View Label (PDF only)]
•    1-oz. individual units of “Country Meats HOT BBQ Flavor Smoked Pork Snack Sticks In Colored Casing Smoke Flavoring Added” with best-by date “11/06/2021”.
The products bear establishment number “EST. 17433” inside the USDA mark of inspection. These items were sold online to individual customers who further sold the product as a fundraiser item.
FSIS is concerned that some product may be in consumers’ pantries.
The problem was discovered when the producing establishment received consumer complaints reporting cheese in the Hot BBQ flavored snack sticks. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
Consumers with food allergies who have purchased these products are urged not to consume them. These products should be thrown away.

Tesoros Trading Company Recalls Product Because of Possible Health Risk

December 16, 2020

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Tesoros Trading Co. from Las Vegas, NV is recalling certain codes of frozen “Trader Joe’s Lightly Salted Edamame” because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled "Trader Joe’s Lightly Salted Edamame” were sold at Trader Joe’s retail stores only in the Arizona, Southern California, Southern Nevada, and Utah regions. All affected product has been removed from sale and destroyed.
The product comes in a 16 ounce plastic package and is stamped on the back bottom portion of the package with lots:
22LA102 M
or 
22LA102 N
or
22LA102 P
The company has removed the affected lots from distribution as the FDA and the company continue to investigate the source of the problem.
Consumers who have purchased 16 ounce packages of "Trader Joe’s Lightly Salted Edamame" with the affected codes are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at (702)706-5263 Monday-Friday 8am - 4:30pm PST. 

George DeLallo Co., Inc. Issues Allergy Alert on Undeclared Pecans in 20 oz Publix Bakery Holiday Cookie Platters

December 8, 2020

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George DeLallo Co., Inc. of Mt. Pleasant, PA is recalling Publix Bakery 20 OZ Holiday Cookie Platters because they may contain undeclared pecans. People who have allergies to pecans run the risk of serious or life-threatening allergic reaction if they consume these products.
The recalled Publix Bakery 20 OZ Holiday Cookie Platters were distributed in Florida, Georgia, Alabama, Tennessee, South Carolina, North Carolina and Virginia. Publix locations in Florida counties Miami-Dade, Palm Beach, Broward and Monroe are NOT impacted by this recall.
The product comes in a 20 ounce, clear plastic package with UPC 41415 88690, marked with lot W34326 and best by date of 10/APR/2021 on the top.
No illnesses have been reported to date in connection with this problem.
The recall was initiated after it was discovered that the pecan-containing product was distributed in packaging that did not reveal the presence of pecans. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's packaging processes.
Consumers with allergies to pecans who have purchased 20 OZ Publix Bakery Holiday Cookie Platters with lot code W34326 are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-433-9100 or 724-925-2222 (Available M-F 8am-5pm, Eastern).

Market of Choice Issues Allergy Alert on Undeclared Almonds in Sour Cherry Baked Brie

December 7, 2020

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Market of Choice of Eugene, Oregon, is recalling its in-house Sour Cherry Baked Brie because of undeclared almonds. Those who have an allergy or severe sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume this product.
Market of Choice Sour Cherry Baked Brie was sold at its Market Cheese Shops in Ashland, Bend, Corvallis, Eugene, Portland, and West Linn in Oregon between 11/1/20 and 12/4/20. No related illnesses have been reported to date.
The affected product is wrapped in a plastic shrink wrap and has a white adhesive store label (see label below). It has the UPC 0 217241 414996 and has the Sell By dates up to and including 12/12/20. The recall was initiated after it was discovered that almonds were present but were not declared on the ingredients list.
Customers who purchased Sour Cherry Baked Brie are urged to discard it if they have an allergy to almonds. This recall is being made with the knowledge of the U.S. Food and Drug Administration and the Oregon Department of Agriculture.
Customers can call with questions 541-345-0566, Ext. 3127, MON-FRI, 8 am-4:30 pm PST.

WishGarden Herbs Issues Voluntary Nationwide Recall of Cord Care and Goldenseal Powder Due to Bacterial Contamination

December 7, 2020

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WishGarden Herbs, Inc. is voluntarily recalling, to the consumer level, 14 lots of Cord Care and Goldenseal Powder products produced after 7/26/18 with expiration dates between 7/26/18 and 9/1/20. After receiving notice of a supply chain issue, WishGarden has determined these products were manufactured using ingredients potentially contaminated with Cronobacter sakazakii bacteria.
Use of these products, when contaminated with this bacteria, may cause serious infections with severe outcomes, including death, especially in vulnerable patients with compromised immune systems and infants.
Catherine Hunziker, WishGarden President, stated, “As a leading herbal product company for more than 40 years, we take the safety of our products seriously and we feel it is important to recall this product out of an abundance of caution. Consumer safety is our highest priority.”
Cord Care Powder is marketed to dry umbilical cords and is applied externally to skin. It is packaged in 1oz containers and labeled with UPC 6-56490-24730-4. The affected product lots are P227-P235. The lot and expiration date can be found below the label barcode.
Goldenseal Powder is marketed as a drying powder applied externally to skin. It is packaged in 1oz containers and labeled with UPC 6-56490-64137-9. Affected product lots are P116-P120. The lot and expiration date can be found below the label barcode.
These products were distributed nationwide in the USA through select practitioners.
WishGarden Herbs has notified its distributors and customers by phone, mail and email. Consumers who have purchased this recalled product should discontinue use immediately and not open any sealed packages. The product should be mailed directly to WishGarden Herbs corporate headquarters at 321 South Taylor Ave. Suite 100 Louisville, CO 80027 for a full refund.
Consumers with questions regarding this recall can contact WishGarden Herbs by calling the company’s recall hotline at 720-889-9878 (M-F, 9am - 5pm MST) or Email: recall@wishgardenherbs.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this product.

Flowers Foods Issues Voluntary Recall of Two Canyon Bakehouse Products Due to Possible Presence of Gluten

December 7, 2020

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Flowers Foods, Inc. (NYSE: FLO) is recalling certain Canyon Bakehouse Mountain White Bread and Canyon Bakehouse Everything Bagels due to the potential presence of gluten. Consumption of this product by people with a wheat allergy, celiac disease, or gluten or wheat sensitivity may cause adverse health effects or serious allergic reactions.
The products being recalled were distributed to retail customers in Arkansas, Colorado, Kansas, Louisiana, Mississippi, Missouri, Montana, Nebraska, New Mexico, Oklahoma, South Dakota, Texas, Utah, and Wyoming. The recall was initiated after finished product testing revealed the possible presence of gluten.
No related illnesses or incidents have been reported to date. Following is information about the products involved in the recall. People should not consume products if both the UPC and Lot Number are noted on the package. The Lot Number is printed on the plastic closure that seals the bag.
Product    UPC    Lot Number
Canyon Bakehouse Mountain White Bread    8-53584-00200-3    032220323
Canyon Bakehouse Everything Bagels    8-53584-00221-8    032220316
Consumers should discard affected product or return it to the place of purchase for a full refund. Consumers with questions may call Flowers’ Consumer Relations Center at 1-866-245-8921. The center is open Monday through Friday from 8:00 a.m. to 5:00 p.m. EST. Consumers also may contact the center via e-mail by visiting www.flowersfoods.com/contact/consumers.

Continental Glatt Kosher Meats Corp. Recalls Ready-To-Eat Meat and Poultry Products Produced Without Benefit of Inspection

December 7, 2020

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Continental Glatt Kosher Meats Corp., doing business as First Choice Kosher Meat & Deli Inc., a Spring Valley, N.Y. firm, is recalling approximately 61,504 pounds of ready-to-eat (RTE) meat and poultry products that were produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The RTE meat and poultry items were produced on various dates from June 26, 2020, through Nov. 20, 2020, with various sell-by dates ranging from October 2, 2020, through April 18, 2021. The products subject to the recall can be found on the following spreadsheet. [View Labels (PDF Only)]       
The products subject to recall bear establishment number “EST. 40009” inside the USDA mark of inspection. These items were shipped to retail locations in New York.        
The problem was discovered when the New York State Department of Agriculture and Markets alerted FSIS about meat and poultry products produced by Continental Glatt Kosher Meats Corp., without the benefit of federal inspection and bearing the mark of inspection from another establishment without authorization.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.  
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Abraham Gruenzweig, Production Manager, Continental Glatt Kosher Meats Corp at (845) 659-4733.

MPM Medical LLC Issues Voluntary Nationwide Recall of Regenecare HA Hydrogel Due to Burkholderia cepecia Contamination

December 3, 2020

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Mesquite, TX MPM Medical is voluntarily recalling one lot of Regenecare HA Hydrogel to the consumer level. Following two customer complaints of visible contamination, the product was found to be contaminated with the bacteria Burkholderia cepecia.
Risk Statement: Topical application of Regenecare HA Hydrogel contaminated with B. cepacia may result in local skin infections. For immunocompromised patients, including patients receiving chemotherapy and patients with cystic fibrosis, the skin infection is more likely to spread into the blood stream leading to life-threatening sepsis which includes symptoms such as fever, difficulty breathing, low blood pressure, fast heart rate, mental confusion and possibly death. To date, MPM Medical has not received any reports of adverse events related to this recall.
Regenecare HA Hydrogel is an OTC product that contains 2% lidocaine and is used topically for temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites or minor skin irritations and is packaged in 3 oz. plastic tubes and distributed in boxes of 12. The product can be identified by NDC # 66977-107-03, and the lot number 41262 with date 2021-01 debossed on the tube crimp as shown in the images below. Regenecare HA Hydrogel Lot 41262 was distributed nationwide to wholesalers and healthcare facilities.
MPM Medical is notifying its distributors and customers by first class mail, electronic mail, and phone call and is arranging for return of all recalled product. Patients and healthcare facilities in possession of this product which is being recalled should stop using and dispensing.
Consumers with questions regarding this recall can contact MPM Medical by phone at 1-800-232-5512 (toll-free) Monday through Friday between 7AM and 5PM CST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
MPM Medical is committed to delivering safe, fully compliant products of the highest quality and is taking necessary steps to prevent future occurrence of this issue.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Hong Thai Foods Corp Issues Allergy Alert on Undeclared Milk Allergens in Golden Boy Custard Muffin Original

December 3, 2020

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Hong Thai Foods Corp. of Brooklyn, NY is recalling its 7.76 ounce packages of Golden Boy Custard Muffin Original because they may contain undeclared milk allergens and are adulterated with Uranine- Acid Yellow 73. Consumers who are allergic to milk allergens may run the risk of serious or life-threatening allergic reactions if they consume this product.
The recalled Golden Boy Custard Muffin Original were distributed nationwide in retail stores. The product comes in a 7.76 ounce, rigid clear plastic package marked with Best Before date of 29/01/2022 on the bottom. The product UPC code is 9555719731581.
No illnesses or allergic reactions involving this product have been reported to date.
The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of undeclared milk allergens in the 7.76 ounce packages of Golden Boy Custard Muffin Original which did not declare a milk ingredient on the label.
Consumers who have purchased 7.76 ounce packages of Golden Boy Custard Muffin Original are urged to, not eat it, throw it out or return them to the place of purchase for a full refund. Consumers with questions may contact the company at (718) 237-1511.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hong-thai-foods-corp-issues-allergy-alert-undeclared-milk-allergens-golden-boy-custard-muffin?utm_medium=email&utm_source=govdelivery

Maribel’s Sweets Issues Allergy Alert on Undeclared Milk Allergen in Product

December 1, 2020

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Maribel’s Sweets of Brooklyn New York is recalling its 5oz Cacao Market Cylinder Dark Chocolate Pearls, because they contain undeclared milk. People who have an allergy or severe sensitivity to milk, run the risk of serious or life-threatening allergic reaction if they consume this product.
This product was distributed locally in our point of sale in New York City stores (484 Broome and 66 Park Avenue) and in all 50 States in United States through our website sales MarieBelle.com. The Cacao Market by MarieBelle dark chocolate pearls are packaged in a 5oz plastic cylinder with UPC 877708002502. The scope of the recall is for all Cacao Market Cylinder Dark Chocolate Pearls within expiry that does not list milk on the label.
No illness nor allergic reactions involving this product have been reported to date.
The recall was initiated after it was discovered that product containing milk was distributed in packaging that did not reveal the presence of milk. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's production and packaging processes.
Consumers who have purchased the 5oz. Cacao Market Cylinder Dark Chocolate Pearls with UPC code 87708002502 are instructed to discard said product immediately or return it to the store for a refund.
Consumers with questions may contact the company at 718-599-5515 Monday – Friday 9-5pm EST.
Other products with a different UPC code also contain milk which is correctly indicated on the labels.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/maribels-sweets-issues-allergy-alert-undeclared-milk-allergen-product?utm_medium=email&utm_source=govdelivery

Vegpro International Issues a Recall of Fresh Attitude Baby Spinach Because of Potential Salmonella Health Risk

November 29, 2020

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Vegpro International of Sherrington, QC CAN is recalling Fresh Attitude baby spinach (5oz and 11oz) with Best before dates of Dec 4th (for 11oz) and Dec 4th & 5th (for the 5oz), because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis
These products were produced in Vegpro’s Eastern Canadian plant and have been distributed ONLY in Eastern Canada and in the Northeastern United States (NY,NJ, DE, CT,MD & PA ). All other Fresh Attitude product sold in the US is produced in Belle-Glade Florida and is not linked to this recall whatsoever and therefore safe for consumption.
No illnesses have been reported to date.
The recall was initiated after it was discovered that the product was possibly contaminated with Salmonella subsequent investigation indicates that the problem may have been caused by contamination of a part of a lot of  Baby Spinach.
Veg Pro recalled due to health risk
•    BABY SPINACH. 8 X 5 OZ, Fresh Attitude, Best before 2020-12-04 & 2020-12-05
UPC : 888048000042
UPC case : 10888048000049
•    BABY SPINACH. 9 X 11 OZ, Fresh Attitude, Best before 2020-12-04
UPC : 888048000288
UPC case : 10888048000285
Consumers who have purchased these products are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1-877-613-5700 or on our website at: http://vegpro.com/contact/

Tarantino Wholesale Foods Distributor Recalls Ready-to-Eat Chicken Breast Products That May be Undercooked

November 29, 2020

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Tarantino Wholesale Foods Distributor, a San Diego, Calif., establishment, is recalling approximately 1,115 pounds of ready-to-eat chicken breast products due to undercooking, resulting in the potential survival of bacterial pathogens in the products, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The ready-to-eat grilled chicken breast items were produced on October 23, 2020. The following products are subject to recall: [View Label]
•    10-lb. cases of “MARY’S FULLY COOKED CHICKEN BREAST” with lot code 20297 and use by date 10/23/21.
The cases containing the products subject to recall bear establishment number “P-8119” inside the USDA mark of inspection. These items were shipped to institution locations in California and were sold directly to retail consumers.            
The problem was discovered when the firm received a customer complaint that the ready-to-eat chicken product appeared to be undercooked.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.      
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.        
Consumers with questions regarding the recall can contact Marcos Tarantino, Quality Assurance Supervisor, at marcos.tarantino@tarantinosausage.com. Media with questions regarding the recall can contact Pete Tarantino, CEO, at (619) 232-7585.

Riverside Natural Foods LTD. Issues Allergy Alert on Undeclared Almond in "Good & Gather Banana Chocolate Chip Date & Nut Bar"

November 25, 2020

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Riverside Natural Foods, of Vaughan, ON is voluntarily recalling its 8 ounce packages of " Good & Gather Banana Chocolate Chip Date & Nut Bar " because they were improperly labelled and may contain undeclared almonds. The product is labelled to may contain tree nuts; however, people who have allergies to almonds may experience a serious or life-threatening allergic reaction if they consume these products.
The recalled " Good & Gather Banana Chocolate Chip Date & Nut Bar " were distributed nationwide in retail stores and through mail orders.
The product comes in a 8 ounce, carton package marked with lot # 1020 on the bottom and with an expiration date of 13 JUL 2021 stamped on the bottom.
No illnesses have been reported to date in connection with this issue.
The recall was initiated after it was discovered that the almond-containing product was distributed in packaging that did not reveal the presence of almonds. Subsequent investigation indicates the issue was caused by an error in the company's packaging processes.
Consumers who have purchased 8 ounce packages of " Good & Gather Banana Chocolate Chip Date & Nut Bar " are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Riverside Natural Foods at 1-416-360-8200 ex 226.

Prairie Farms Issues Allergy Alert on Undeclared Egg in Chocolate Milk Gallons

November 25, 2020

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Prairie Farms has issued a limited voluntary recall of its Prairie Farms Premium Flavored Chocolate Milk gallons and Prairie Farms 1% Lowfat Chocolate Milk gallons (Best by Date: Dec. 4, 2020) that were not labeled for an egg allergen that may be present. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume these products.
A total of 1,152 units of chocolate milk gallons (355 units of Premium Flavored Chocolate and 797 units of 1% Lowfat Chocolate) were distributed at retail outlets in the Chicago area, including the Northern Illinois Suburbs, Rockford, Illinois, and Southeastern Wisconsin. The recalled products contain the following code dates and UPC#’s: 
•    One Gallon Prairie Farms Dairy Premium Flavored Chocolate Milk
UPC: 72730-26110
Best by Date: Dec. 4, 2020
Plant Code: 17-284
•    One Gallon Prairie Farms Dairy
1% Lowfat Chocolate Milk
UPC: 72730-26126
Best by Date: Dec. 4, 2020
Plant Code: 17-284
The recall was initiated after cross-contamination with egg nog was discovered following a valve malfunction at the Rockford, Illinois plant. No illnesses have been reported to date. Prairie Farms Chocolate Milk gallons produced at plants, other than Rockford, Ill. plant Code 17-284, including Premium Flavored Chocolate, 1% Lowfat Chocolate, 2% Reduced Fat Chocolate, and Fat Free Chocolate, are not part of this recall.
Prairie Farms Dairy is currently working in partnership with the FDA to fully investigate the matter and comply with all necessary recall procedures. Prairie Farms is also establishing preventive measures to address the issue and apologizes for any inconvenience caused by this product issue.
Customers who have purchased this product are encouraged to destroy the product or return it to their local retailer to exchange the product for a like item. Consumers with questions may contact Prairie Farms Dairy at 618-659-5700 or info@prairiefarms.com, Monday through Friday, 8:00 a.m. to 4:00 p.m. Central Time.

Hy-Vee Voluntarily Recalls Two Short Cuts Vegetable Mix Products Because of Possible Health Risk

November 25, 2020

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Hy-Vee, Inc., based in West Des Moines, Iowa, is voluntarily recalling two of its Hy-Vee Short Cuts vegetable mix products across its eight-state region (IL, IA, KS, MN, MO, NE, SD, and WI) due to possible contamination with Listeria monocytogenes. The potential for contamination was discovered during routine safety sampling at Hy-Vee’s Short Cuts production facility. To date, no illnesses have been reported in connection with these products.
Listeria monocytogenes is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria monocytogenes infection can cause miscarriages and stillbirths among pregnant women.
Out of an abundance of caution, Hy-Vee is recalling the following products from all of its stores:
•    Hy-Vee Short Cuts Pot Roast Mix – UPC Code 0272083305352
•    Hy-Vee Short Cuts Grill/Oven Ready Veggie Mix – UPC Code 0272104105992
All affected products have a “Best if Used By” date of Dec. 3, 2020. Photos of the affected product labels are attached. No other Hy-Vee Short Cuts products or products used in Hy-Vee stores are affected by this recall.
Customers who purchased any of these products with these dates should not consume them. Customers are being asked to discard these items or return them to their local Hy-Vee store for a full refund.
Consumers with questions may contact Hy-Vee Customer Care representatives 24 hours a day, seven days a week at (800) 772-4098.

Shenandoah Growers Inc Issues a Limited, Voluntary Recall of Certain Imported Organic Basil Because of Potential Health Risk

November 25, 2020

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Shenandoah Growers, Inc (Harrisonburg, VA) out of an abundance of caution, has issued a limited, voluntary recall of approximately 15,000 units in select packages, due to a possible health risk from Cyclospora.
These were packed under branded and private label fresh cut organic certified basil clamshells at its Jefferson, GA facility and Harrisonburg, VA facility with the following lot codes, all with the country of origin of Colombia. Recalled products were distributed to select retail stores between 10/20/2020 and 10/30/2020 in various states including Georgia, Tennessee, Florida, Virginia, Pennsylvania, Maryland, Connecticut, Delaware, New Jersey, New York, and Washington DC.
Affected lot codes:
LOT Number:    Brand:    Size:    UPC:
PV14334C296    The Fresh Market    0.5oz    7-37094-23027-2
PV64308E304    Good & Gather    0.5oz    0-85239-12215-0
PV64308C296    Naturally Better    0.5oz    6-07880-20230-4
PV64308A300    Naturally Better    0.5oz    6-07880-20230-4
PV64308D300    Naturally Better    0.5oz    6-07880-20230-4
PV14334E297    Nature’s Promise    4.0oz    6-88267-16220-6
PV14334E297    Nature’s Promise    2.5 oz    6-88267-54893-2
PV14334E297    Nature’s Promise    0.5oz    6-88267-19910-3
PV14334B296    Nature’s Promise    0.5oz    6-88267-19910-3
PV14334C297    O Organics    0.66oz    0-79893-98072-0
PV 14334E297    O Organics    4.0oz    0-79893-98081-2
PV64308B294    Simple Truth    3.0oz    0-11110-00876-3
PV64308D297    Simple Truth    3.0oz    0-11110-00876-3
PV64308E295    That’s Tasty    3.0oz    7-68573-53001-9
PV64308E296    That’s Tasty    2.0oz    7-68573-51510-8
PV64308A298    That’s Tasty    3.0oz    7-68573-53001-9
PV14334C296    Wild Harvest    0.25oz    7-11535-50450-4
PV14334C296    Wild Harvest    4.0oz    7-11535-50323-1
PV14334C296    Wild Harvest    2.0oz    7-11535-50762-8
The Shenandoah Growers recall includes only those clamshells of certified organic basil clearly marked with the affected lot codes listed above. The lot code can be found printed on each clamshell.
This precautionary recall notification is being issued due to an isolated instance in which a package pulled by the Florida Department of Agriculture on 11/2/2020 from a retail store in Florida indicated the potential presence of Cyclospora.
Affected Shenandoah Growers customers have been notified of the recall and instructed to immediately remove and discard recalled products from all store shelves, distribution and other inventories to ensure they are no longer available for sale or consumption.
These products were harvested and packed nearly 4 weeks ago and should no longer be in commerce.
Cyclosporiasis is an intestinal infection caused by the Cyclospora parasite. A person may become infected after ingesting contaminated food or water. Common symptoms include severe abdominal pain, diarrhea, nausea and vomiting, body aches and fatigue. The infection is treated with antibiotics and most people respond quickly to treatment.
No other Shenandoah Growers products are subject to recall, and the company has no knowledge of any illness reported or related to this product.
Consumers who may have a recalled basil product should discard it immediately and not eat it. Consumers with questions, or to obtain refunds, may contact the Shenandoah Growers Consumer Response Center at 844-896-6939 Monday through Friday, 8 am to 5 pm Eastern time.
Shenandoah Growers takes food safety matters very seriously, and stringently follows all mandated regulations and implements preventive measures designed to minimize potential risks. Shenandoah Growers is working in close coordination with regulatory officials, including the FDA, on this matter.

Fusion Health and Vitality Issues Voluntary Nationwide Recall of Core Essential Nutrients and Immune Boost Sublingual Vitamin D3 Due to the Unapproved Use of a Food Additive and Unapproved Marketing Statements

November 24, 2020

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Fusion Health and Vitality LLCis voluntarily recalling all 2020 Lots of CORE essential nutrients and Immune Boost Sublingual Vitamin D3. CORE has been found to contain an unapproved food additive, hordenine HCl, rendering it adulterated. Immune Boost Labeling was found to contain statements that caused it to become and unapproved new drug under FDA labeling laws. Hordenine HCl is possibly unsafe when taken by mouth. Hordenine HCl might have similar stimulant effects and side effects such as rapid heart rate and high blood pressure.
Fusion Health and Vitality LLC has not received any reports of adverse events related to this recall.  Please review the attached photos for identification.
We began shipping Core Essential Nutrients on 1/2/2020 and we began shipping Immune Boost Sublingual Vitamin D3 on 4/15/2020.
Both products are packaged with labels which prominently display the product name.  CORE essential nutrients are found in a dark colored jar, in powdered format.  This product was formulated to mix into a liquid before consumption.
The Immune Boost sublingual was packaged in a 2 ounce bottle that came with a sublingual application dropper.
Fusion Health and Vitality is notifying its customers by email and is arranging for return of all recalled products.
Consumers that have product which is being recalled should stop using it and return it to Fusion Health and Vitality for destruction.
Consumers with questions regarding this recall or how to return recalled product can contact Fusion Health and Vitality by calling 1-888-964-5327, 9am to 5pm, Monday Thru Friday, EST.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

FSIS Issues Public Health Alert for Chicken and Beef Samosa Products Containing Pastry Ingredients That Have Been Recalled Due to Misbranding

November 23, 2020

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The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for chicken and beef samosa products containing spring roll pastries that have been recalled by the manufacturer, Tee Yih Jia (TYJ) Food Manufacturing, due to misbranding and an undeclared allergen. The products may contain milk, a known allergen, which is not declared on the product labels. FSIS is issuing this public health alert out of the utmost of caution to ensure that consumers are aware that these products should not be consumed. A FSIS recall was not requested because the Food and Drug Administration (FDA) inquiry for the spring roll pastry recall is ongoing. As more information becomes available, FSIS will update this public health alert. 
The chicken and beef samosas items were produced from November 11, 2019 through November 11, 2020. The following products are subject to the public health alert: [View Labels (PDF only)]
•    12-oz. packages containing 12 pieces of “TAZA CHICKEN SAMOSAS Stuffed pastry with seasoned chicken” with best by dates of November 11, 2020 through November 11, 2021.
•    12-oz. packages containing 12 pieces of “TAZA BEEF SAMOSAS Stuffed pastry with seasoned ground beef” with best by dates of November 11, 2020 through November 11, 2021.
•    12-oz. packages containing 12 pieces of “SOUTH ASIAN FOOD Beef SAMOSAS Stuffed pastry with seasoned ground beef” with best before dates of November 11, 2020 through November 11, 2021.
•    12-oz. packages containing 12 pieces of “SOUTH ASIAN FOOD Chicken SAMOSAS Stuffed pastry with seasoned chicken” with best before dates of November 11, 2020 through November 11, 2021.
The products bear establishment number “EST. 44163” or “P-44163” inside the USDA mark of inspection. These items were shipped to distributors in California, New York and Texas.
The problem was discovered during routine FSIS verification activities. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

Dole Fresh Vegetables Announces Limited Recall of Organic Romaine Hearts

November 21, 2020

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Dole Fresh Vegetables, Inc. is voluntarily recalling a limited number of cases of organic romaine hearts. The products being recalled are Dole™ Organic Romaine Hearts 3pk (UPC 0-71430-90061-1), combined English/French packaging, with Harvested-On dates of 10-23-20 and 10-26-20, and Wild Harvest Organic Romaine Hearts (UPC 7-11535-50201-2), with Harvested-On dates of 10-23-20 and 10-26-20.  The recall is being conducted due to a possible health risk from E. coli in the two products.  Dole Fresh Vegetables is coordinating closely with regulatory officials. No illnesses have been reported to date in association with the recall. 
Pathogenic E. coli can cause diarrhea, severe stomach cramps and vomiting.  Most people recover within a week, but some illnesses can last longer and can be more severe.
The Harvested-On sticker is located on the upper right corner of each bag and the UPC code is located on the bottom right corner of the back of each bag. The Dole package contains three organic romaine hearts and the Wild Harvest product is packaged in a 12oz bag. The impacted products were distributed in AZ, HI, IA, IL, IN, KS, MD, MI, MN, MO, MS, MT, NC, ND and VA. These products were harvested and packed nearly 4 weeks ago and should no longer be in commerce.  Consumers are advised to check product they have in their homes and discard any product matching the production description, UPC codes and Harvested-On dates listed above.
This precautionary recall notification is being issued due to an isolated instance in which a package of Dole™ Organic Romaine Hearts – 3pk yielded a positive result for pathogenic non-O157 E.coli STEC in a routine sample collected at a retail store by the Michigan Department of Agriculture and Rural Development. There is no indication at this time that this positive result is related to any illnesses nor consumer complaints and it is not associated with the strains connected to the ongoing outbreaks currently under regulatory investigation. 
No other Dole products are included in the recall. This voluntary recall does not apply to any bagged or clamshell salad romaine product. Only the specific Organic Romaine Hearts listed, with the exact UPC codes and Harvested-On dates identified above, are included in the recall. Consumers who have any remaining product with these UPC codes and Harvested-On dates should not consume it, but rather discard it. Retailers and consumers with questions may call the Dole Consumer Center at 1-800-356-3111, which is open 24 hours a day.

Fresh Express Recalls Limited Quantity of Expired Fresh Express Kit Caesar Supreme Due to Potential Health Risk

November 19, 2020

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Fresh Express is voluntarily recalling a limited number of cases of expired 10.5 oz. Fresh Express Kit Caesar Supreme with the Use-by Date of November 8, 2020 and Product Code S296 because it may be contaminated with Escherichia coli STEC 026 bacteria. The recall is being executed out of an abundance of caution in the unlikely event the product, which is now 8 days past the Use-By Date, is still in stores or consumers’ homes. The recalled product was distributed primarily in Western and Southwestern U.S. states.
No illnesses are reported, and no consumer complaints have been received by the Fresh Express Consumer Response Center in association with this recall.  No other Fresh Express products are subject to recall.
The recall of the expired product is being conducted due to an isolated incident in which a single randomly selected package of 10.5 oz. Fresh Express Kit Caesar Supreme yielded a positive result for E. coli STEC 026.
E. coli STEC 026 can cause diarrhea, severe stomach cramps and vomiting.  Most people recover within a week, but some illnesses can last longer and can be more severe.
Consumers who may still have the expired product at home in their refrigerators should discard and not consume it.  For questions or to obtain refunds, consumers may  call the Fresh Express Consumer Response Center tollfree at (800) 242-5472 during the hours of 8 a.m. to 7 p.m. Eastern time.  Refunds are also available where purchased.
Fresh Express is conducting this recall in coordination with the U.S. Food and Drug Administration.
Recall Specifics: 
•    Product Being Recalled: 10.5 oz. Fresh Express Kit Caesar Supreme with Product Code S296 and Use-By Date NOV 8, located in upper right corner on the front of the package and UPC Code 0 7127930104 4 on the reverse side of the package.  
•    Possible Distribution: Alaska, Arizona, California, Colorado, Hawaii, Idaho, Montana, North Dakota, New Mexico, Nevada, Oregon, Texas, Utah, Washington and Wyoming.
 
Recall: Fresh Express Kit Caesar Supreme Issued on 11/16/20
(No other Fresh Express salads are included in this recall)
BRAND    PRODUCT NAME    SIZE    UPC    PRODUCTION CODE    USE BY DATE    POSSIBLE DISTRIBUTION STATES
Fresh Express    Fresh Express Kit Caesar Supreme      10.5-oz.    0 7127930104 4    S296    NOV 08    AK, AZ, CA, CO, HI, ID,
MT, ND, NM, NV, OR, TX, UT, WA, WY

Kanan Enterprises Conducts Voluntary Recall of ALDI Southern Grove On the Go Sweet & Salty Trail Mix Due to Undeclared Almonds

November 12, 2020

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On the Go Sweet & Salty Trail Mix 
Out of an abundance of caution Kanan Enterprises announces the voluntary recall of ALDI Southern Grove On the Go Sweet & Salty Trail Mix 8 Pack Caddies 1.5 oz., Best By JUL 27 2021 due to the presence of almonds that are not listed as ingredients.  People who have an allergy to almonds run the risk of a serious or life-threatening allergic reaction if they consume these products. No illnesses have been reported associated with this recall.
The only item that is affected by this recall is ALDI Southern Grove On the Go Sweet & Salty Trail Mix a 1.5 ounce pouch bag with a UPC 4099100005202 and a date code of Best By JUL 27 2021.  No other products or date codes are affected.  Product was distributed Aldi stores in the states of CT, DE, FL, MA, MD, NH, NJ, NY, PA, RI, VA, VT, WV.
We were notified by a customer that almonds were packaged in bags of ALDI Southern Grove On the Go Sweet & Salty Trail Mix.
Consumers with this reported product should not consume this product.  They should destroy it.  Consumers with questions should call 1-800-860-5464, 8:15 am – 5:00pm EST, Monday – Friday.

FSIS Issues Public Health Alert for Chicken and Pork Tamales Containing FDA-Regulated Diced Tomatoes in Puree That Have Been Recalled Due to Possible Foreign Matter Contamination

November 16, 2020

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The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) chicken and pork tamale products containing Food and Drug Administration (FDA) regulated diced tomatoes in puree that have been recalled by the producer, due to concerns that the products may be contaminated with extraneous materials, specifically hard plastic. The hard plastic may pose a choking hazard or cause damage to teeth or gums. FSIS is issuing this public health alert out of the utmost of caution to ensure that consumers are aware that these products, which bear the USDA mark of inspection, should not be consumed.
The frozen RTE chicken and pork tamale items were produced between Oct. 22, 2020 and Nov. 9, 2020 by Tucson Tamale Wholesale Co. LLC, an establishment in Tucson, Ariz.  The following products are subject to the public health alert: [View Labels (PDF only)]
•    Cases containing eight individually packed tamales with the labels “TUCSON TAMALE GREEN CHILE CHICKEN TAMALE” or “TUCSON TAMALE Green Chile Chicken Tamales” with lot codes F20296 and F20309 and sell by dates of 10/23/22 and 11/05/22.
•    Cases containing six packages with two tamales each of “TUCSON TAMALE GREEN CHILE CHICKEN TAMALES” with lot codes F20309 and F20296 and sell by dates of 10/23/22 and 11/05/22.
•    Cases containing 30 tamales of “TUCSON TAMALE Green Chile Pork & Cheese Tamales” with lot codes F20303 and F20307 and sell by dates of 10/30/22 and 11/03/22.
•    Cases containing eight individually packed tamales of “TUCSON TAMALE GREEN CHILE PORK & CHEESE TAMALE” with lot codes F20307 and F20314 and sell by dates of 11/03/22 and 11/10/22.
•    Cases containing six packages with two tamales each of “TUCSON TAMALE GREEN CHILE PORK & CHEESE TAMALES” with lot codes F20303 and F20307 and sell by dates 10/30/22 and 11/03/22.
•    Packages containing two tamales of “TUCSON TAMALE GREEN CHILE PORK & CHEESE TAMALES” with lot codes F20303, F20307 and F20302 and sell by dates of 10/29/22, 10/30/22 and 11/03/22.
•    Cases containing 30 tamales of “TUCSON TAMALE Green Chile Chicken Tamales” with lot code F20296 and sell by date of 10/23/22.
The products bear establishment number “EST. 45860” inside the USDA mark of inspection. These items were sold online and also shipped to distributors for further distribution to retail locations and restaurants nationwide.
The problem was discovered by Tucson Tamale Wholesale Co. when they identified pieces of hard plastic in the cans of diced tomatoes in puree that they received from their ingredients supplier. The ingredients supplier initiated a recall of the diced tomatoes in puree with the FDA. As more FDA information becomes available, FSIS will update this public health alert.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Consumers and members of the media with questions can contact Sherry Martin, CEO of Tucson Tamale Wholesale Co., at (520) 398-6282.

Homestead Creamery Issues Voluntary Glass Bottled Product Recall

October 30, 2020

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Homestead Creamery of Wirtz, VA is voluntarily recalling glass bottled products because of a suspected issue with the bottle sanitizing process. Glass bottled product in question may have a strong sanitizer odor which may affect the taste and quality of the product. There is no known health risk associated with the issue at this time.
Affected products include:
Product    UPC    Best Buy Dates
A2A2 2% half gallon    875252000289    Nov 8
Creamline Whole Milk half gallon    875252000074    Nov 4, Nov 8, Nov 9
Homogenized Whole Milk half gallon    875252000173    Nov 4, Nov 8, Nov 9
Homogenized Whole Milk quart    875252000159    Nov 5, Nov 8, Nov 9
2% Milk half gallon    875252000272    Nov 4, Nov 8, Nov 9
2% Milk quart    875252000258    Nov 4, Nov 8, Nov 9
Non-Fat Creamline Milk half gallon    875252000371    Nov 4, Nov 8, Nov 9
Non-Fat Creamline Milk quart    875252000357    Nov 8, Nov 9
Chocolate Milk half gallon    875252000470    Nov 4, Nov 8, Nov 9
Chocolate Milk quart    875252000456    Nov 4, Nov 5, Nov 9
Orange Cream Milk quart    875252000623    Nov 8
Cowpuccino Milk quart    875252000760    Nov 8
Heavy Cream quart    875252000890    Nov 4, Nov 8, Nov 9
Half and Half quart    875252000869    Nov 8, Nov 9
Buttermilk quart    875252000821    Nov 29
Lemonade half gallon    875252002658    Dec 19, Dec 20
Eggnog quart returnable bottle    875252000982    Nov 15
Old Fashioned Custard quart returnable bottle    875252000920    Nov 15
Eggnog half gallon returnable bottle    875252000999    Nov 15
Eggnog quart nonreturnable bottle    875252001002    Nov 15
Old Fashioned Custard quart nonreturnable bottle    875252000951    Nov 15
These returnable glass bottles were distributed in Virginia, West Virginia, North Carolina, South Carolina, Georgia, Alabama, Ohio, Pennsylvania, Maryland, New Jersey, and New York in October through retail stores, direct delivery, and wholesale distributors. Shipments of this product started on October 15, 2020.
Eggnog and custard round, non-returnable glass bottles with the best by date of Nov 15 were distributed to The Fresh Market stores in Alabama, Arkansas, Connecticut, Delaware, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Maryland, Massachusetts, Mississippi, New Jersey, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, and Virginia. Shipments of this product started on October 14th, 2020.
The best by date of the bottle is located on the side of the bottle cap. No serious illnesses have been reported to date in connection with this problem.
The recall was initiated after it was discovered that product smelled like cleaning agent.
Consumers should return the bottles to the place of purchase for a full refund. The recall should be carried out to the user level. Consumers with questions may contact the company at 540-721-2045 Monday- Friday 8:00am-4:30pm Eastern Time.

Russ Davis Wholesale Issues Allergy Alert on Undeclared Egg in Mixed Veggie Cup With Dip

October 28, 2020

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Russ Davis Wholesale of Wadena, Minnesota is recalling individual serving cups of Mixed Veggie Cup with Dip because it may contain undeclared Egg. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume these products.
The Mixed Veggie Cup with Dip was distributed in Colorado, Kansas, South Dakota, Wyoming, New Mexico in higher education, health care and corporate campus’ in grab ‘n go coolers.
Product is labeled J&O Mixed Veggie Cup with Dip in a 5.0 oz plastic container with a Sell By date of 9/30/20 through 11/2/20.
No illnesses have been reported to date.
The issue was discovered by Quality Control team during a routine label audit, where egg was noted on the dressing ingredient and was not reflected on the finished product label.
Consumers who have purchased Mixed Veggie Cup with Dip should dispose of the product. Consumers many contact Customer Service at 877-433-2173.

Allergy Alert Issued for Undeclared Egg in Prepared Macaroni & Cheese Sold at Whole Foods Market Stores in Five States

October 28, 2020

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Whole Foods Market is voluntarily recalling select prepared Macaroni & Cheese products from stores across five states because they contain undeclared egg. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume these products.
The affected products were sold at Whole Foods Market stores in Maryland, New Jersey, Pennsylvania, Virginia and Washington, D.C. The product was sold in plastic containers and in family-style meal kits with Whole Foods Market scale labels in the prepared foods department, available both hot and refrigerated. The product was also available from the chef’s case counter and from Whole Foods Market online and catering menus. The affected products can be identified by the following information.
All affected product has been removed from store shelves. No allergic reactions have been reported to date.
Product    Product Code (begins with)M    Best by date through
Macaroni & Cheese, chef’s case    286501    10/28/2020
Macaroni & Cheese, packaged    263608    10/27/2020
Macaroni & Cheese, online and catering    114449
109866    10/23/2020
Rotisserie Chicken Meals with Mac & Cheese and Broccoli, packaged    261596
261580
261590
261601
261608
261616    10/26/2020
Fried Chicken Meal with Mac & Cheese, packaged    247257    10/25/2020
Fried Chicken Meal with Mac & Cheese, packaged on hot bar    237444    10/24/2020
Chicken Rustico Romano Chef Plate with Mac & Cheese and Broccoli, packaged    241442    10/28/2020
Chicken Breast Chef Plate with Mac & Cheese and Broccoli, packaged    299430    10/28/2020
BBQ Turkey Meatballs Chef Plate with Mac & Cheese and Green Beans, packaged    241464    10/28/2020
Roasted Turkey Chef Plate with Mac & Cheese and Broccoli, packaged    242019    10/28/2020
Customers who purchased this product at Whole Foods Market can bring a valid receipt into stores for a full refund. Consumers with additional questions can call 1-844-936-8255 between the hours of 7:00 a.m. and 10:00 p.m. CST, Monday through Friday, or 8:00 a.m. and 6:00 p.m. Saturday through Sunday.

Allergy Alert Issued By Incredible Fish, Inc. for Undeclared Milk, Fish and Eggs in Incredible Stone Crab Mustard Sauce

October 24, 2020

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Incredible Fish, Inc. is voluntarily recalling a small quantity of Incredible Stone Crab Mustard Sauce because its labeling inadvertently did not identify the following allergens in the product: milk, fish, and eggs.  People who have an allergy or severe sensitivity to milk, fish, or eggs run the risk of a serious or life-threatening allergic reaction if they consume this product.
Incredible Stone Crab Mustard Sauce was sold to a limited number of consumers between October 15, 2020 and October 22, 2020, primarily through the company’s website. Customers who purchased products directly from Incredible Fish have all been notified directly of the recall. There is a potential that some direct customers of Incredible Fish may have re-sold this product at retail stores within the state of Florida.
The product is packaged in 8 oz. containers that display the words: “Incredible Stone Crab Mustard Sauce.”
Customers with allergies or sensitivities to milk, fish, or eggs should discard the product or contact Incredible Fish to return it for a full refund.
To date, no illnesses related to this product have been reported. Incredible Fish is working collaboratively with the U.S. Food and Drug Administration on this recall.
Incredible Fish takes seriously the safety and integrity of the products it distributes and regrets any inconvenience and concern this recall may cause.
Customers who have any questions about the recall may contact Carlos Figueroa at carlos.figueroa@incrediblefish.com or by phone at (305) 696-7183 from 8:00 a.m. – 5:00 p.m. EST Monday through Friday.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/allergy-alert-issued-incredible-fish-inc-undeclared-milk-fish-and-eggs-incredible-stone-crab-mustard?utm_medium=email&utm_source=govdelivery

Orca Bay Foods, LLC Issues Allergy Alert on Undeclared Wheat and Milk Allergens in Gluten Free Battered Halibut

October 23, 2020

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Orca Bay Foods of Seattle, WA is recalling 4,450 lb. (356 cases) of 10 oz. retail box Trader Joe's brand Gluten Free Battered Halibut SKU 00503822, because it contains undeclared wheat and milk allergens. People who have an allergy or severe sensitivity to wheat and milk run the risk of serious or life-threatening allergic reaction if they consume this product.
Product was sold in Trader Joe's stores in Connecticut, Illinois, Indiana, Iowa, Kansas, Kentucky, Maine, Massachusetts, Michigan, Minnesota, Missouri, Nebraska, New Hampshire, New York, Ohio, Rhode Island, Tennessee, Vermont, and Wisconsin. 
Trader Joe's brand Gluten Free Battered Halibut SKU 00503822 product is packed in 10 oz retail carton boxes, and the affected code 537312620 Best If Used By Nov 5, 2021 is located on box end.
No illnesses have been reported to date.
The recall was initiated after it was discovered that product containing Wheat and Milk was distributed in packaging that did not reveal the presence of the allergens.
This recall is being undertaken with the knowledge of the U.S. Food and Drug Administration.
Consumers who have purchased are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-932-ORCA, Monday-Friday, 8 am-4:30 pm PST.

Comercial Mexicana International Inc. Recalls “Tropique Assorted Fruit Jelly Bag 30/9PCS/10.06oz and Tropique Jelly Animal Jar 6/26oz ” Due to Possible Health Risk

October 22, 2020

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Comercial Mexicana International Inc. in Bethpage New York is recalling the product because it may pose a choking hazard. Small jelly cups containing seaweed extract (carrageenan) has been identified as a potential choking hazard in children
No incidents of consumers choking have been reported to date in connection with this problem. The potential choking hazard was discovered during a routine inspection by the New York State Department of Agriculture and Markets, Food Safety and inspection.
The recalled jelly cups were sold in NY, NJ, CT, PA retail stores.
The recall products are:
Description    UPC    GRAMS    PACKAGED    BEST BEFORE    CUPS
TROPIQUE ASSORTED FRUIT JELLY 30/9PCS/10.6oz    732068496333    301    PLASTIC BAG    9/17/2021    9
TROPIQUE JELLY ANIMAL TIGER JAR 6/26OZ    732068496050    737    PLASTIC JAR    1/18/2022    22
TROPIQUE JELLY ANIMAL OWL JAR 6/26OZ    732068496012    737    PLASTIC JAR    1/18/2022    22
TROPIQUE JELLY ANIMAL DUCK JAR 6/26OZ    732068495992    737    PLASTIC JAR    1/18/2022    22
TROPIQUE JELLY ANIMAL BEAR JAR 6/26OZ    732068496098    737    PLASTIC JAR    1/18/2022    22
TROPIQUE JELLY ANIMAL PANDA JAR 6/26OZ    732068496036    737    PLASTIC JAR    1/18/2022    22
TROPIQUE JELLY ANIMAL PIG JAR 6/26OZ    732068496074    737    PLASTIC JAR    1/18/2022    22
TROPIQUE JELLY ANIMAL CAT JAR 6/26OZ    732068496111    737    PLASTIC JAR    1/18/2022    22
The product is packaged in a Plastic Green Bag with fruit design on the front, with 9 individual plastic jelly cups inside each pack. The second product is a Jelly jar packaged in a Plastic Jar with an animal shape. It has 22 individual plastic jelly cups inside each container. The UPC number on the products are all listed above. The Container code marked on the package is “best before” 09/17/2021 for TROPIQUE ASSORTED FRUIT JELLY BAG and ‘best before”01/18/2022” for TROPIQUE JELLY ANIMAL JAR.
If you purchased this product, do not eat it and don’t give it to your children. Return them to the store where you purchased them, or throw them away in a sealed package inside a secure garbage can with a tight-fitting lid.

Taher, Inc. Recalls Meat Products Produced Without Benefit of Inspection

October 17, 2020

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Taher, Inc., a Plymouth, Minn. firm, is recalling approximately 22,096 pounds of meat products that were produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The frozen meat products were produced and packaged from Feb. 25, 2020 through Sept. 22, 2020. The following products are subject to recall: [View Labels (PDF Only)]
•    16-lb. boxes containing 4 bags of “Fresh Seasons Tator Tot Hot Dish” with lot code 056-282 and barcode 108101060239.
•    16-lb. boxes containing 4 bags of “Fresh Seasons Sloppy Joe” with lot code 065-269 and barcode 1081010602366.
The products subject to recall may or may not bear establishment number “EST. 45091” inside the USDA mark of inspection. These items were shipped to institutions and food service locations in Minnesota.
The problem was discovered by FSIS’ inspection personnel who determined that the products were produced without the benefit of federal inspection.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS is concerned that some product may be in institutional or food service freezers. Institutions and food service locations who have purchased these products are urged not to serve them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Jill Teut, director of communications at Taher, Inc. at (612) 708-0350.

Hadson Toko Trading Co., Inc. Recalls Eishindo Mini Cup Jelly (50pcs) Because of Potential Choking Hazard

October 14, 2020

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HADSON (TOKO) TRADING CO., INC. OF MASPETH, NY is recalling its 28.2oz (800g) bags of EISHINDO MINI CUP JELLY (50 pcs) (迷你果凍杯(大)) due to the product being a potential choking hazard based off of its product size and consistency. Small jelly cups have previously been implicated in choking deaths of children.
The recalled jelly cups were distributed nationwide in retail food stores and are sold in large clear bags of 50 jelly cups. The UPC code is, “4970481000034,” Product code is, “E007.”
No incidents of consumers choking have been reported to date in connection with this product.
The potential choking hazard was noted after discussion with a representative from the Food and Drug Administration.
Consumers who have purchased 28.2oz (800g) bags of EISHINDO MINI CUP JELLYS are urged to return them to the store where they were purchased for a full refund or throw them away in a sealed package inside a secure garbage can with a tight fitting lid. Consumers who have questions or concerns may contact the company at 718-628-6761 Monday thru Friday between 8AM and 6PM EST.

Red Monkey Foods, Inc. Recalls Parsley and Herbes De Provence Because of Possible Health Risk

October 13, 2020

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Red Monkey Foods, Inc. out of an abundance of caution is voluntarily recalling select organic parsley as part of a recall initiated by High Quality Organics (HQO). HQO has issued a recall for a lot of parsley because a sample was tested by one of HQO’s customers and was found to be potentially contaminated with Salmonella. A portion of the lot recalled by HQO was supplied to Red Monkey Foods, Inc and subsequently repacked into consumer containers for parsley and was also used to manufacture herbes de provence which was then sold in consumer containers. To date, there have been no consumer complaints or reported cases of Salmonellosis in connection with these products.
Salmonella can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections, endocarditis and arthritis.
The potentially affected product consists of retail packages weighing 0.3-0.65 oz.
The "Best By" date information can be found on the square bottom of the glass bottle. No other "Best By" dates are being recalled.
Item Number    Product Name    Package Size    Product UPC    Production Lot    Product Dates
533310-06    Cost Plus World Market Herbes De Provence    0.6 oz    2533 3107    2552005C    BEST BY 13 MAR 2023
533325-06    Cost Plus World Market Organic Parsley    0.3 oz    2533 3251    2662003D    BEST BY: 24 MAR 2023
GV5451-24    Great Value Herbes De Provence Organic    0.6 oz    0 78742 15451 0    2562001C    BEST IF USED BY MAR 14 2023
GV5460-24    Great Value Organic Parsley Flakes    0.3 oz    0 78742 15460 2    2532002J    BEST If Used By: MAR 11 2023
14200102-24    O Organics Herbes De Provence Organic    0.65 oz    0 79893 41131 6    2662001J    BEST If Used By: MAR 24 23
14200099-05    O Organics Parsley Organic    0.3 oz    0 79893 41109 5    2672001D    BEST If Used By: MAR 25 23
32831-06    Full Circle Parsley Organic    0.3 oz    0 36800 32831 0    2532001J    Best By: 11 MAR 2023
The products in question were distributed to all fifty states and Puerto Rico. The product was produced for sale at retail.
Consumers who have purchased the product with the listed "Best By" dates are urged not to consume the product, but to discard it or return it to the place of purchase for a full refund. Consumers or Media with questions may call our Customer Service Center at (417) 319-7300 or by e-mail at customerservice@redmonkeyfoods.com for more information. Customer Service will be available in person from 8am to 5pm CST Monday to Friday.
Red Monkey Foods, Inc. is committed to providing food safe, high-quality products and the safety and satisfaction of our consumers is the company's utmost priority. Although there have not been any reported cases of Salmonellosis, we are voluntarily recalling the products listed as a preventive measure.

B&G Foods Issues Voluntary Allergy Alert for a Limited Number of Boxes of Back to Nature® Organic Rosemary & Olive Oil Stoneground Wheat Crackers Containing Peanut Butter Cookies

October 9, 2020

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B&G Foods announced today it is voluntarily recalling a very limited number of boxes of a single date code of 6 oz. Back to Nature Organic Rosemary & Olive Oil Stoneground Wheat Crackers, with a “best by” date of APR 25 2021, after learning that a very limited number of the cracker boxes were inadvertently filled with foil wrapped pouches of peanut butter cookies, which contain peanut, an allergen undeclared on the label. People who have an allergy or severe sensitivity to peanut run the risk of serious or life-threatening allergic reaction if they consume the cookies contained in the recalled boxes. There is no health risk associated with this product for individuals without an allergy to peanut.
This recall affects only a very limited number of boxes of the following product, which may have been distributed in retail stores nationwide:
Description    Consumer UPC #    Size    Best By Date
Back to Nature Organic Rosemary & Olive Oil Stoneground Wheat Crackers    8-19898-01015-8    6 oz.    APR 25 2021
(The “best by” date is located on the top of the box.)
This recall does not apply to any other “best by” dates, sizes or varieties of Back to Nature products.
No allergic reactions related to this matter have been reported to date. This recall was initiated in cooperation with the FDA and the third party co-packer that produced the product.
B&G Foods discovered this issue when it received consumer complaints that the foil bags within two boxes of Back to Nature Organic Rosemary & Olive Oil Stoneground Wheat Crackers contained peanut butter cookies. The foil bags do correctly indicate whether the product contains rosemary & olive oil crackers or peanut butter cookies.
A third party co-packer inadvertently used a small number of Back to Nature Organic Rosemary & Olive Oil Stoneground Wheat Crackers product boxes in connection with a production run of peanut butter cookies. Back to Nature Organic Rosemary & Olive Oil Stoneground Wheat Crackers were not produced on that date. As such, B&G Foods believes this recall impacts only a handful of boxes of Back to Nature Organic Rosemary & Olive Oil Stoneground Wheat Crackers. However, out of an abundance of caution, B&G Foods is issuing this recall for boxes with this particular “best by” date that have been shipped to its customers. Product with this particular “best by” date may have been shipped and distributed by B&G Foods to its customers’ warehouses located in Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Maryland, Maine, North Carolina, New Hampshire, New Jersey, Nevada, New York, Ohio, Pennsylvania, Tennessee, Texas, Washington and Wisconsin.
Consumers who have purchased the recalled product can return it to the place of purchase for a full refund. Consumers seeking a refund or additional information may also contact B&G Foods by calling 855.346.2225 Monday through Friday from 8:30 a.m. to 6:00 p.m. Eastern time.

Sauer Brands, Inc. Voluntarily Recalls Certain The Spice Hunter Products Because of Potential Salmonella Contamination

October 12, 2020

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Sauer Brands, Inc. is voluntarily recalling The Spice Hunter Products listed below due to the potential presence of Salmonella. After initially certifying that our raw material had tested negative for Salmonella, and was fit for human consumption, our supplier notified us of the potential presence of salmonella in specific lots of organic parsley that it provided to us. Those lots of parsley were used on two specific days in our production. We are recalling other products produced on those same days out of an abundance of caution regarding potential cross contamination.
While Sauer is aware of no reports of illness to date, that relate to these products, Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. If you are experiencing these symptoms, and believe you may have been exposed to Salmonella, please report to a medical provider.
The Spice Hunter Products in question were distributed to the states of Alaska, Alabama, Arizona, California, Colorado, Delaware, Florida, Georgia, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maryland, Michigan, Missouri, North Carolina, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington and Wisconsin. The product was produced for sale at retail and spicehunter.com
These products come in clear glass jars marked with lot codes 20217C, 20220C, 20269C and 20270C on the white field on the label. A list of the products is shown below:
1.3 ounce 1.6 ounce 
Item Num    Product Name    Brand Name    Jar UPC    Case UPC    Lot Number    Best By Date    Description    Product Size
41659    Organic Parsley    The Spice Hunter    8105701659    40081057016594    20217C    Aug-22    Parsley Flakes    0.23 ounce
41659    Organic Parsley    The Spice Hunter    8105701659    40081057016594    20269C    Sep-22    Parsley Flakes    0.23 ounce
41245    Saigon Organic Cinnamon    The Spice Hunter    8105701245    40081057012459    20217C    Aug-22    Ground Cinnamon    1.7 ounce
41260    Madagascar Cloves    The Spice Hunter    8105701260    40081057012602    20220C    Aug-22    Ground Cloves    1.9 ounce
41937    Gourmet Sesame Seeds    The Spice Hunter    8105701937    40081057019373    20220C    Aug-22    Sesame seeds    2.4 ounce
41440    Herbes De Provence    The Spice Hunter    8105701440    40081057014408    20220C    Aug-22    French Herb Blend    0.6 ounce
41850    Pumpkin Pie Spice    The Spice Hunter    8105701850    40081057018505    20220C    Aug-22    Pumpkin pie spice    1.8 ounce
41935    Seafood Grill & Broil    The Spice Hunter    8105701935    40081057019359    20220C    Aug-22    Seafood seasoning blend    1.3 ounce
41275    Coriander    The Spice Hunter    8105701275    40081057012756    20220C    Aug-22    Ground Coriander    1.4 ounce
41400    California Garlic    The Spice Hunter    8105701400    0081057014002    20220C    Aug-22    Granulated Garlic    2.7 ounce
42256    Green Hatch Chile    The Spice Hunter    8105702256    40081057022564    20220C    Aug-22    green chile    2.4 ounce
41541    Mexican Seasoning    The Spice Hunter    8105701541    40081057015412    20269C    Sep-22    Organic Mexican Spice blend    1.4 ounce
41703    Black Pepper    The Spice Hunter    8105701703    40081057017034    20269C    Sep-22    Coarse Ground Black Pepper    1.7 ounce
41653    Paprika    The Spice Hunter    8105701653    40081057016532    20269C    Sep-22    Organic Paprika    1.4 ounce
41955    Szechwan Seasoning    The Spice Hunter    8105701955    40081057019557    20269C    Sep-22    Chinese Seasonin Blend    2.1 ounce
41706    Fine Black Pepper    The Spice Hunter    8105701706    40081057017065    20269C    Sep-22    Fine Ground Black Pepper    1.6 ounce
41420    Chinese Ginger    The Spice Hunter    8105701420    40081057014200    20269C    Sep-22    Ginger    1.6 ounce
41792    Muntock White Pepper    The Spice Hunter    8105701792    40081057017928    20269C    Sep-22    White Pepper    2.1 ounce
41402    Roasted Garlic    The Spice Hunter    8105701402    40081057014026    20269C    Sep-22    Roasted Granulated Garlic    2.2 ounce
41351    Everything Bagel Crunch    The Spice Hunter    8105701351    40081057013517    20270C    Sep-22    Bagel Seasoning Blend    2.3 ounce
41700    Malabar Black Peppercorns    The Spice Hunter    8105701700    40081057017003    20270C    Sep-24    Black Peppercorns    2.1 ounce
41230    Freeze-Dried Chives    The Spice Hunter    8105701230    40081057012305    20270C    Sep-23    Green Chives    0.13 ounce
41450    Italian Seasoning    The Spice Hunter    8105701450    40081057014507    20270C    Sep-22    Mediterranean Herb Blend    0.6 ounce
41236    Cilantro    The Spice Hunter    8105701236    40081057012367    20270C    Sep-22    Organic Cilantro    0.3 ounce
41363    Fennel Seeds    The Spice Hunter    8105741363    40081057413630    20270C    Sep-24    Whole Fennel Seeds    1.3 ounce
41348    Dill Weed    The Spice Hunter    8105701348    40081057013487    20270C    Sep-22    Organic Dill Weed    0.5 ounce
41050    Arrowroot    The Spice Hunter    8105701050    40081057010509    20270C    Sep-22    Ground Arrowroot    2.1 ounce
41170    Cayenne Red Pepper    The Spice Hunter    8105701170    40081057011704    20270C    Sep-24    Cayenne Red Pepper    1.8 ounce
41440    Herbes De Provence    The Spice Hunter    8105701440    40081057014408    20270C    Sep-22    French Herb Blend    0.6 ounce
Consumers who have purchased The Spice Hunter products on this list are urged to avoid consuming them and return them to the place of purchase for a full refund. Consumers with questions may contact Sauer Brands, Inc. at 1-800-444-3061, Monday thru Friday, from 8:30 AM to 4:00 PM.

Country Fresh Expands Voluntary Recall 

October 3, 2020

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Country Fresh is extending their voluntary recall issued on October 2, 2020 to include various containers of “Freshness Guaranteed “cut and/or sliced apples, grapes, mangos, pineapples and cantaloupe distributed by Walmart. The recall is a precautionary measure due to a possible health risk from Listeria monocytogenes detected on equipment used in an area near where these products are packed. FDA discovered these findings during a recent inspection.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recall affects product codes of various fresh fruit items shipped directly to Walmart retail distribution centers and sent to select stores located in AR, IL, IN, KS, KY, LA, MO, OK, and TX. The products were packaged in various size clam shell containers (see photos). The “best if used by” dates are between October 3, 2020 and October 11, 2020 and the products are as follows:
UPC    Item Description    Best if used by:
68113118012    APPLE GRAPE TRAY w/ CARMEL 2 lbs 10oz    10/7/2020    10/8/2020    -
68113118006    GREEN APPLE SLICES 32oz    10/8/2020    10/9/2020    10/10/2020
68113118007    MIXED APPLE SLICES 32oz    10/8/2020    10/9/2020    10/10/2020
68113118004    RED APPLE SLICES 14oz    10/10/2020    10/11/2020    -
68113118010    RED APPLE SLICES 32oz    10/8/2020    10/9/2020    -
68113118014    CANTALOUPE CHUNKS 10oz    10/3/2020    10/4/2020    10/5/2020
68113118015    CANTALOUPE CHUNKS 16oz    10/3/2020    10/4/2020    10/5/2020
68113118023    SEASONAL FRUIT TRAY 40oz    10/3/2020    10/4/2020    -
68113135509    SUMMER BLEND 5oz    10/3/2020    10/4/2020    -
68113135510    TROPICAL BLEND 5oz    10/3/2020    10/4/2020    -
68113118037    MANGO CHUNK 10oz    10/3/2020    10/4/2020    -
68113118038    MANGO SPEARS 16oz    10/4/2020    -    -
68113118039    PINEAPPLE GRAPE MANGO BLEND 16oz    10/3/2020    10/4/2020    10/5/2020
68113118042    PINEAPPLE CHUNKS 10oz    10/3/2020    -    -
68113118046    PINEAPPLE CHUNKS 16oz    10/4/2020    -    -
68113118043    PINEAPPLE CHUNKS 42oz    10/10/2020    10/11/2020    -
68113118044    PINEAPPLE SPEARS 32oz    10/5/2020    -    -
68113118047    RED GRAPES 10oz    10/4/2020    -    -
68113118048    SEASONAL BLEND 10oz    10/3/2020    10/4/2020    -
68113118049    SEASONAL BLEND 16oz    10/3/2020    10/4/2020    10/5/2020
68113118050    SEASONAL BLEND 32oz    10/5/2020    -    -
68113118069    SEASONAL TRIO 32oz    10/3/2020    10/4/2020    10/5/2020
Country Fresh has not received any reports of illnesses to date. Walmart retail stores are removing the recalled product from store shelves and inventories immediately. Customers who have any recalled product on the list should not consume it and discard it immediately.
This recall is being undertaken with the knowledge of the U.S. Food and Drug Administration.
Country Fresh takes food safety matters very seriously, stringently follows all mandated regulations and implements preventive measures designed to minimize potential risks. Country Fresh is working in close coordination with FDA in its continuing investigation to resolve the matter promptly and deeply regrets the inconvenience to our consumers and customers.
If you have any questions, please contact Customer Service at: 1-877-251-8300 Monday – Friday 8 AM to 5PM CST

Meijer Recalls Whole Cantaloupes and Select Cut Cantaloupe Trays Due to Potential Health Risk 

October 7, 2020

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Meijer, in conjunction with Eagle Produce, LLC in Aguila, AZ., is announcing a voluntary recall of whole cantaloupe and select cut cantaloupe fruit trays and bowls. The recall is part of a sampling investigation by the Michigan Department of Agriculture and Rural Development and is due to the potential risk of Salmonella.
Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
The multi-state recall involves whole cantaloupe and select cut cantaloupe fruit trays and bowls in various weights ranging from 6–40 ounces sold between Sept. 26 and Oct. 5 of this year at all Meijer stores in Michigan, Ohio, Indiana, Illinois, Kentucky and Wisconsin. There have been no illnesses reported to date.
The recalled whole cantaloupe would have a sticker label stating Kandy Brand from Eagle Produce, LLC. If there is no sticker label to identify it, then it should be considered part of the recall. In addition, Meijer may have used cantaloupe ingredients that originated from Eagle Produce, LLC in the store made products. The following packaged products are in clear plastic containers under the Meijer brand label include:
9450 – Gas Station Mixed Melon Chunk Cup
9505 – Gas Station Mixed Fruit Cup 
9644 -  Gas Station Cantaloupe  6 oz
21921000000 – Fruit Frenzy Bowl 40 oz
21921400000 – Fruit Tray 
21924800000 – Fruit Tray with Dip
21932300000 – Cantaloupe Chunks Large PLU 4960
21933400000 – Mixed Melon Chunks Large Bowl
21933700000 – Mixed Melon Chunks Small Bowl
21960100000 – Fruit Frenzy 16 oz Bowl PLU
21971100000 – Strawberry/Pineapple Cup 6 oz
21971200000 – Mixed Fruit Cup 6 oz
21971700000 – Berry Explosion Cup 6 oz
21971800000 – Mixed Melon Chunk Cup 6 oz
21984400000 – Mixed Melon Cup 
22012400000 – Mixed Fruit Cup
22019600000 – Cantaloupe Chunks Small Bowl
22020000000 – Fruit Frenzy 32 oz Bowl PLU 1
22021900000 – Cantaloupe and Honeydew Slices
22022000000 – Mixed Melon Slices
22045000000 – Fruit Palooza
22045200000 – Melons & Berries
22045300000 – Triple Treat & Melon
22061600000 – Cantaloupe Chunks Large Kosher
22061700000 – Cantaloupe Chunks Large Kosher
28873400000 – Fruit Salad
 Consumers who have purchased this product should throw it away or return the product to the nearest Meijer store for a full refund. Consumers with questions regarding this recall should contact Meijer at 800-543-3704, available 24 hours a day, seven days a week. Consumers with questions or concerns about their health should contact their physician.

Ashtel Studios Issues Voluntary Recall of Licensed Hand Sanitizers Packaged in 0.84 Fluid Ounce Pouches Due to Misbranding Because They Resemble Food and Drink 

October 2, 2020

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Ashtel Studios has announced a voluntary recall of all lots of licensed hand sanitizer packaged in .84 oz containers resembling food and drink pouches labeled with various children’s characters listed in the table below to the consumer level. The products are being recalled because they are packaged in containers resembling food and drink pouch. The recall does not affect any other Hand Sanitizer products from Ashtel Studios.
Product    Size    NDC
PAW Patrol Hand Sanitizer    0.84 FL. OZ (25 mL)    70108-042-01
JoJo Siwa Hand Sanitizer    0.84 FL. OZ (25 mL)    70108-044-01
Hot Wheels Hand Sanitizer    0.84 FL. OZ (25 mL)    70108-045-01
Barbie Hand Sanitizer    0.84 FL. OZ (25 mL)    70108-046-01
Trolls Hand Sanitizer    0.84 FL. OZ (25 mL)    70108-047-01
Minions Hand Sanitizer    0.84 FL. OZ (25 mL)    70108-043-01
Ingesting hand sanitizer, which is intended for topical use, could potentially result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal. Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute. Ashtel Studios has received no reports of adverse reactions
The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available and is packaged in 0.84 oz pouches. The product can be identified by examples of the products pictured below.  Product was distributed to selected retailers in the United States and Canada.  
Ashtel Studios has provided written notification to its distributors and retailers and is alerting customers via this voluntary recall. While the product is not available for purchase, if a consumer has product which is being recalled they are advised to destroy it immediately.
Consumers with questions regarding this recall can contact Ashtel Studios, 866-Ashtel-1, 909-434-0911 (international) from 9:00 am-5:00 pm PST
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Seneca Recalls Cinnamon Apple Chips Because of Possible Health Risk

October 2, 2020

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Seneca Snack Company, a Washington Corporation, is announcing a voluntary recall of Seneca Cinnamon Apple Chips and Clancy’s Cinnamon Apple Chips due to possible Salmonella contamination.
Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting in the bloodstream and producing more severe illnesses such as arterial infections, endocarditis and arthritis.
This recall is only for specific cinnamon flavor lot codes, no other flavor apple chips are affected. This only affects Clancy’s product sold by ALDI and Seneca products sold nationwide through Amazon and Gemline, no other retailers are affected.
Seneca is not aware of any reports of consumer illness related to this product.
Seneca was notified by an ingredient supplier that it shipped one lot of ingredients containing cinnamon that has the potential to be contaminated with Salmonella. In response to that notification; Seneca is now retrieving Cinnamon Apple Chips from its distribution system.
The recall extends to the following labels and package sizes ONLY:
Seneca Cinnamon Apple Chips 0.7 ounce Package
UPC: 0 18195-70140 4
-Individual Package Codes:
26JUN2021
Seneca Cinnamon Apple Chips 2.5 ounce Package
UPC: 0 18195-70100 8
-Individual Package Codes:
28JUN2021
Clancy’s Cinnamon Apple Chips 2.5 ounce Package
-Individual Package Codes:
26JUN2021
27JUN2021
Consumers with this product should return it for a full refund to the retail outlet where it was purchased. Consumers who want more information may call Seneca Foods Consumer Affairs at 1-800-872-1110.

Country Fresh Voluntary Product Recall

October 1, 2020

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Country Fresh is initiating a voluntary recall of a limited quantity of watermelon chunks from select stores as a precautionary measure due to a possible health risk from Listeria monocytogenes detected on equipment used in packing this product. FDA made these findings during a recent inspection.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recall affects product codes of watermelon items shipped directly to Walmart and RaceTrac’s retail distribution centers stores in select stores located in Arkansas, Missouri, Illinois, Oklahoma, and Texas. The product was packaged in a variety of clam shell containers (see photos). The best-if-used by dates of October 2, 3, and 4, 2020 and the SKUs are as follows:
Walmart – Freshness Guaranteed
Watermelon 4 x 10 oz – UPC Code: 681131180672
Watermelon 2 x 32 oz – UPC Code: 681131180672 Watermelon Chunks 2 x 42 oz – UPC Code: 681131180658 Watermelon Spears 4 x 16 oz – UPC Code: 681131180665 Summer Blend FTC 4 x 5 oz – UPC Code: 681131355094
RaceTrac
Watermelon 5.5oz – UPC Code: 74641000644 Melon Trio 5.5oz – UPC Code: 74641031945
Country Fresh has not received any reports of illnesses to date associated with these recalled items. The recalled products were distributed from 9/23/2020 – 9/25/2020. RaceTrac and Walmart retail stores are removing the recalled product from store shelves and inventories immediately. Customers with recalled watermelon should discard it immediately and not consume it.
This recall is being undertaken with the knowledge of the U.S. Food and Drug Administration.
Country Fresh takes food safety matters very seriously, stringently follows all mandated regulations and implements preventive measures designed to minimize potential risks. Country Fresh is working in close coordination with FDA in its continuing investigation to resolve the matter promptly and deeply regrets the inconvenience to our consumers and customers. If you have any questions, please contact Customer Service at: 1-877-251-8300 Monday – Friday, 8-5pm CST
Watermelon 32oz, Lot URR0103, Use By 10/2/20
Watermelon 32oz, Lot URE0103, Use By 10/3/20
Watermelon 42oz, Lot URR0103, Use By 10/2/20
Watermelon 42oz, Lot URE0103, Use By 10/3/20
Watermelon 16oz, Lot URR0103, Use By 10/2/20
Watermelon 16oz, Lot URS0103, Use By 10/4/20
Watermelon 10oz, Lot URR0103, Use By 10/2/20
Watermelon 10oz, Lot URE0103, Use By 10/3/20
Watermelon 10oz, Lot URS0103, Use By 10/4/2
Watermelon 5.5oz, Lot URE0103, Use By 10/4/20
Summer Blend 5oz, Lot URR0103, Use By 10/2/20
Summer Blend 5oz, Lot URE0103, Use By 10/3/20
Summer Blend 5oz, Lot URS0103, Use By 10/4/20
Melon Trio 5.5oz, Lot URE0103, Use By 10/4/20

DMM VISSION, S.A. DE C.V. Issues Voluntary Nationwide Recall of Cleaner Hand Sanitizer 500 mL and 1200 mL Bottles Due to the Possible Presence of Undeclared Methanol (Wood Alcohol)

September 30, 2020

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Estado de México, México, DMM VISSION, S.A. de C.V. is voluntarily recalling five lots of Cleaner Hand Sanitizer, 500 mL and 1,200 mL plastic clear bottles with white tops currently in US distribution to the consumer level. This recall is being initiated out of abundance of caution due to detection of methanol (wood alcohol) in hand sanitizer sample manufactured at the same facility.
Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date DMM VISSION has not received reports of adverse events related to this recall.
The product is used as a hand sanitizer and are packaged in 500ml and 1200ml plastic clear bottles with white tops. The lot numbers are LC2020407, LC2020408, LC2020502, LC2020504, LC2020507.  This product was first distributed nationwide to wholesale distributors on April 27, 2020 and finished on June 9th, 2020. The recalled products are as follows:
Product(s)    Country of Origin    Product Size    Product Label    Lot number    NDC    Expiry Date
Cleaner Hand Sanitizer    Mexico    1200 ML    See Product Image Below    LC2020407    75799-000-04    April/2021
Cleaner Hand Sanitizer    Mexico    500 ML    See Product Image Below    LC2020408    75799-000-02    April /2021
Cleaner Hand Sanitizer    Mexico    1200 ML    See Product Image Below    LC2020502    75799-000-04    May/2021
Cleaner Hand Sanitizer    Mexico    1200 ML    See Product Image Below    LC2020504    75799-000-04    May/2021
Cleaner Hand Sanitizer    Mexico    1200 ML    See Product Image Below    LC2020507    75799-000-04    May/2021
DMM VISSION is notifying its distributors by phone calls, emails and/or mailed letters and is arranging for return of all recalled products. Consumers, distributors, and retailers that have product which is being recalled should stop use or distribution and return to place of purchase.
Consumers with questions regarding this recall can contact DMM VISSION by phone (+52) 5547578351 or email to dmmvissionrecall@yahoo.com on Monday through Friday from 9 am and 5 pm, CST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Consumers/distributors/retailers that have the above listed lots Cleaner Hand Sanitizer should stop using or distributing the products immediately and mail the products to 700 County Line Rd., Lakewood, NJ, 08701.
Contact Name: José Álvarez
Phone Number: (+52) 5547578351

Wismettac Asian Foods Voluntarily Recalls Dried Fungus Due to Potential Salmonella Contamination

September 23, 2020

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Wismettac Asian Foods, Inc., Santa Fe Springs, CA is issuing a voluntary recall for Shirakiku brand imported Dried Fungus (also known as Black Fungus or Kikurage) because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
The product was distributed to restaurants in Arkansas, California, Colorado, Connecticut, Delaware, Washington DC, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nevada, New Jersey, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, Wisconsin and British Columbia in Canada.
•    Affected Product:
Item Number    Item Description    Pack Size    UPC Code    Product Lot Code    Package Photo
#60403    BLACK FUNGUS (KIKURAGE) 5LB    5 LB    00074410604035    All Lots with Item #60403 on the package    See below
Wismettac is initiating the recall after the California Department of Public Health discovered the presence of Salmonella in the product. The manufactuer has been made aware of the issue, and is conducting an investigation to determine the cause of the issue so corrections can be implemented.
To ensure consumer safety, all distribution of the affected product has ceased and restaurant customers have been notified for the product removal.
Consumers with questions may contact the company at recall@wismettacusa.com.
Wismettac Asian Foods, Inc.
Food Safety Department
recall@wismettacusa.com

GHSW, LLC Issues Allergy Alert on Undeclared Milk and Egg Allergens

September 21, 2020

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GHSW, LLC. is voluntarily recalling 1512 units of Trader Joe’s Southwest Style Sweet Potato Sauté Bowl due to undeclared milk and egg allergens in the dressing that are not declared on the label. People who are allergic to milk and eggs run the risk of serious or life-threatening allergic reaction if they consume this product.
The dressing is located in a pouch found inside the clear 21.5 oz. bowl. These bowls are sold in the refrigerated section of the store.
The recalled product(s) were shipped to 36 Trader Joe’s stores in the following states: AR, CO, KS, LA, NM, OK, TN, and TX.
The recall has been isolated to only Southwest Style Sweet Potato Sauté Bowl with the Best By dates 09/23/20, 09/24/20, 09/25/20, 09/26/20, and 09/28/20 on the front of the package. No other products or lots are affected by this recall.
No reports of illnesses or injury have been received to date.
The recall was initiated after it was discovered that the dressing containing milk and egg was distributed in packaging that did not declare the presence of milk or egg.
GHSW, LLC is urging customers with any milk and egg allergy concerns to return the product to the point of purchase for a full refund or dispose of the recalled products. GHSW is standing by to answer customer questions at 888-449-9386, M-F, 9 am to 4 pm PST

Homestead Creamery Issues Allergy Alert on Undeclared Pecans in Chocolate Ice Cream Quart

September 21, 2020

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Homestead Creamery of Wirtz, VA is recalling one lot of Homestead Creamery chocolate ice cream quarts, dated 5/13/2021, because it may contain undeclared pecans. People who have an allergy or severe sensitivity to pecans run the risk of serious or life-threatening allergic reaction if they consume these products.
The chocolate ice cream quarts were distributed in Virginia and North Carolina in May through retail stores and direct delivery.
The date of the ice cream is located on the bottom of the container.
No illnesses have been reported to date in connection with this problem.
The recall was initiated after it was discovered that product containing the pecans may have been distributed in packaging that did not reveal the presence of pecans.
Consumers should return the ice cream quart to the place of purchase for a full refund. Consumers with questions may contact the company at 540-721-2045.

Willow Tree Poultry Farm, Inc. Recalls Ready-To-Eat Chicken Salad Products due to Misbranding and an Undeclared Allergen

September 17, 2020

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WASHINGTON, Sept. 16, 2020 – Willow Tree Poultry Farm, Inc., an Attleboro, Mass. establishment is recalling (CLASS 1 RECALL-HIGH RISK) approximately 6,890 pounds of ready-to-eat (RTE) chicken salad products due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products may contain walnuts, a known allergen, which are not declared on the product labels. 
The RTE chicken salad product labeled as “Classic Chicken Salad” may actually contain “White Meat Cranberry Walnut Chicken Salad” and was produced on Sept. 2, 2020. The following product is subject to recall: [View Labels (PDF Only)]
•    15-oz. clear, plastic containers labeled as “Willow Tree Premium White Meat CHICKEN SALAD Classic” with a sell by date of “9/30/20” and a time stamp of 13:00:00 through 17:00:00 on the containers’ cellophane lid.
The products subject to recall bear establishment number “EST. P-8827” inside the USDA mark of inspection. These items were shipped to retail locations in Connecticut, the District of Columbia, Maine, Maryland, Massachusetts, New Hampshire, Rhode Island, Vermont and Virginia.            
The problem was discovered after the firm received a customer complaint reporting walnuts and cranberries were in a container of “Classic” chicken salad.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
FSIS is concerned that some product may be in retailer and consumers’ refrigerators. Retailers who have obtained these products are urged not to sell them. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers with questions about the recall can contact Alex Cekala, Willow Tree Poultry Farm, Inc. General Manager, at ACekala@willowtreefarm.com or at (508) 951-8351. Members of the media with questions about the recall can contact Walter Cekala, Willow Tree Poultry Farm, Inc. President, at WCekala@willowtreefarm.com or at (508) 944-0529.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Goodie Girl Tribeca LLC Recalls Goodie Girl Magical Animal Crackers Due to Undeclared Wheat

September 15, 2020

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Goodie Girl Tribeca LLC announced today it is voluntarily recalling 389 cases of a single date code of 7 oz. Goodie Girl Magical Animal Crackers, with a “best by” date of Jan 11, 21A3, after learning that the product may contain undeclared wheat ingredients. People who have an allergy or severe sensitivity to wheat run the risk of allergic reaction if they consume the product contained in the recalled boxes. There has been an individual with a wheat allergy that was treated for a wheat allergen reaction.
This recall affects only 389 cases of the following product, which were distributed in retail stores nationwide:
Description; Goodie Girl GF Magical Animal Crackers
UPC# 8-5598700395-3
Size; 7 Ounces
Best By Date; Jan 11, 2021
Distributed between 4/17/2020 – 5/7/2020
This recall does not apply to any other “best by” dates, sizes or varieties of Goodie Girl Tribeca LLC.
This recall was initiated in cooperation with the FDA and the third-party co-packer that produced the product.
Product with this particular “best by” date was shipped and distributed by Goodie Girl Tribeca to its customers' warehouses located in Virginia, Pennsylvania, Georgia, New Hampshire, California.
Consumers seeking a refund or additional information may contact info@goodiegirl.com or call 201-941-2000 9am – 5pm est.

Medek, LLC. Issues Voluntary Nationwide Recall of M Hand Sanitizer Due to Potential Presence of Methanol (Wood Alcohol) and Subpotent Ethanol Levels

September 14, 2020

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Medek, LLC is voluntarily recalling all lots of M Hand Sanitizer Alcohol Antiseptic 80% 128 oz/3,785 mL to the consumer level. FDA analysis found the M Hand Sanitizer to contain methanol and be sub-potent for ethanol.
Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. In addition, the use of sub-potent hand sanitizer products can have adverse health consequences related to lack of efficacy and increased risk of infections. To date, Medek, LLC. has not received any reports of adverse.
The recalled product is used as a hand sanitizer for hand washing to decrease bacteria on the skin when soap and water are not available. The recalled Hand Sanitizer is packaged in a one (1) gallon (128 oz/3,785 mL) High-density polyethylene (HDPE) plastic bottle, NDC 75432-001-02.
The recalled Hand Sanitizer was distributed directly to walk-in customers in Alamo, TX, between the dates of 04/17/2020 to 05/22/2020.
Medek, LLC is notifying its customers/distributors by recall letter and consumers via this press release. We are also notifying our distributors, who will help notify their customers by phone calls, emails, and/or mailed letters and is arranging for return of all recalled Hand Sanitizer. Consumers, distributors, and retailers that have recalled products should stop use or distribution and return to place of purchase.
Consumers with questions regarding this recall can contact Medek, LLC at (956) 800-4366 (Monday to Friday from 9 am to 5 pm CST). Consumers should contact their physician or healthcare provider if they experience any problem that may be related to the use of this product.

Cher-Make Sausage Company Recalls Fully Cooked Meat Sausage Products Due to Misbranding and an Undeclared Allergen

September 14, 2020

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Cher-Make Sausage Company, a Manitowoc, Wis. establishment, is recalling approximately 429-lbs of fully-cooked meat sausage products due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains milk (cheese), which is not declared on the packaging label. 
The product labeled as “Old Fashioned Wieners” may contain cheddar wieners product. The product was produced on July 23, 2020. The following products are subject to recall:  [View Labels (PDF only)]
•    5-lb. vacuum sealed packages labeled as “OLD FASHIONED WIENERS COURSE GROUND FULLY COOKED” with sell by date “11/26/20” and lot number “2020503” on the product label.
The products subject to recall bear establishment number “EST. 2420” inside the USDA mark of inspection. These items were shipped to retail locations in Illinois, Minnesota, Nebraska, North Dakota, South Dakota, and Wisconsin and may have been sold intact or from a counter display as individual sausages.                          
The problem was discovered after the firm received a complaint from a store employee who observed cheese in the product.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
FSIS is concerned that some product may be in retailer and consumers’ refrigerators. Retailers who have obtained these products are urged not to sell them. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Tom Chermak, Cher-Make Sausage Company President, at TomC@Cher-make.com or by calling (920) 683-5980.

CorgioMed LLC Issues Voluntary Nationwide Recall of All Lots of Leafree Instant Hand Sanitizer Aloe Vera Labeled as EDIBLE ALCOHOL

September 11, 2020

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CorgioMed, LLC is voluntarily recalling all lots of Leafree Instant Hand Sanitizer-Aloe Vera, within expiry to the consumer level.  The products are being recalled because they are labeled as “EDIBLE ALCOHOL”. Leafree Hand Sanitizer is an alcohol-based hand rub to be applied externally to reduce bacteria on the skin when soap and water are not available.
Risk Statement: Ingesting hand sanitizer, which is intended for topical use, may result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal. Young children may experience a sharp decrease in blood sugar which may result in death. Pregnant women who ingest alcohol have experienced birth defects and developmental disabilities. Nursing mothers who ingest alcohol in above moderate levels may see developmental, growth and sleep pattern damages in their babies and may experience impaired judgement and ability to safely care for their child. Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute.  The labeling of this product as ‘edible alcohol’ may promote this behavior.
The product is used as a hand sanitizer and is packaged in 100 ml (UPC #6970495860325), 300 ml (UPC #69705860318) and 500 ml (UPC #6970495860301) bottles.  Product was distributed Nationwide via CorgioMed website.
CorgioMed LLC is notifying its distributors and customers by email and is arranging for return or disposal of all recalled products.
Distributors and Consumers with questions regarding this recall can contact CorgioMed LLC by emailing to: contact@corgiomed.comor phone: 301-978-3898 from September 1st to September 30th, 2020. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

AJR Trading LLC Issues Voluntary Nationwide Recall of bio aaa Advance Hand Sanitizer 480 mL Bottles, Lot 20DF8307

September 11, 2020

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AJR Trading is voluntarily recalling 2,004 units of lot 20DF8307 of bio aaa Advance Hand Sanitizer currently in US distribution, packaged in 480 mL bottles, to the consumer level.
This lot of bio aaa Advance Hand Sanitizer has been tested and meets all appropriate specifications and tests.
However, in an abundance of caution, these units are being recalled because of possible presence of methanol in other lots of bio aaa Advance Hand Sanitizer.
Risk Statement: Substantial methanol exposure could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Although all persons using these products on their hands may be at risk; young children who accidently ingest them and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.
To date, AJR Trading has not received reports of adverse events related to this recall.
The product is used as a hand sanitizer to reduce bacteria when soap and water is not available and is packaged in 480 mL plastic bottles UPC 7502272121085.  AJR Trading is recalling lot 20DF8307, expiration date April 2022. The product can be identified by the images below. Product was distributed in Miami beginning in April 2020.
AJR Trading is notifying its customers by phone calls, e-mails, and letters.  AJR Trading is arranging for refund and destruction of recalled products. Consumers/distributors/retailers that have the above listed lots of bio aaa Hand Sanitizer, which is being recalled, should stop using or distributing the products immediately and mail the products to AJR Trading at the address below for refund:
814 Ponce de Leon Blvd, suite 218. Coral Gables, FL. 33134.
Consumers with questions regarding this recall can contact AJR Trading by phone insert 305-302-8416 or e-mail to ajrtrading15@gmaill.com Monday to Friday from 10:00 am to 5:00 pm Central Time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Fresco Foods, Inc. Issues Allergy Alert on Undeclared Fish (Anchovies) in Ancient Grain Jackfruit Bowl

September 11, 2020

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Fresco Foods Inc. of Tampa, FL is voluntarily recalling ALL units of ANCIENT GRAIN JACKFRUIT BOWL because it may contain an undeclared allergen, Fish (anchovies). People who have an allergy or severe sensitivity to Fish (anchovies) run the risk of serious or life-threatening allergic reaction if they consume these products.
The Ancient Grain Jackfruit Bowl was distributed in Alabama, Florida, Georgia, North Carolina, South Carolina, Tennessee, and Virginia in retail stores including Natural Foods grocers, independent markets and Publix supermarkets.
No illnesses have been reported to date.
THE FOLLOWING PRODUCTS ARE SUBJECT TO THE ALLERGY ALERT:
Product: Eat Fresco, Ancient Grain Jackfruit Bowl
Product Identification: Product comes in 14 ounces (397 grams) plastic white rectangular tray with skin vacuum seal and is kept refrigerated. Best If Used By/Freeze By: 9/15/2020 and prior.
The allergy alert was initiated after it was discovered that the Ancient Grain Jackfruit Bowl containing Fish (anchovies) was distributed in packaging that did not reveal the presence of Fish (anchovies). Subsequent investigation indicates the problem was caused by sourcing the wrong sub-ingredient.
The product has been discontinued effective immediately. All future production has been cancelled for this item.
Individuals with an allergy or sensitivity to fish (anchovies) should not consume this product. Households that include individuals with an allergy or sensitivity to fish (anchovies) should dispose of the product.
Consumers with questions may contact Tracy Povolny at Fresco Foods, Inc. at 813-551-2100.

Pretty Thai Issues Allergy Alert on Undeclared Peanuts in Mislabeled Peanut Sauce

September 10, 2020

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Pretty Thai of Austin, Texas, is recalling Pretty Thai Peanut Sauce that may have been mislabeled as Pretty Thai Sweet Chili Sauce. There is a risk that a person with an allergy or severe sensitivity to peanuts could unintentionally consume a product containing peanuts because of this error. No illnesses have been reported to date.
The product was distributed to H-E-B and Central Market stores in Texas from March 19, 2020 to September 8, 2020.
The product is packaged in clear, cylindrical PET bottles with black flip-top caps and clear labels with white print. The recall is for Pretty Thai Peanut Sauce with the Lot Code 0772000123. A small number of the Pretty Thai Peanut Sauce bottles were discovered to have been mislabeled as Pretty Thai Sweet Chili Sauce. Pretty Thai Peanut Sauce is yellow or gold in color, while Pretty Thai Sweet Chili Sauce is dark red in color. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume the mislabeled product.
Pretty Thai and its manufacturer, Ponder Foods, have coordinated efforts with H-E-B to remove all of the affected product from the shelves and from distribution. Out of an abundance of caution, we are alerting consumers in Texas who may have purchased either Pretty Thai Peanut Sauce or Pretty Thai Sweet Chili Sauce to check any product for Lot Code 0772000123. For consumers with no peanut allergy, this Lot Code of Pretty Thai Peanut Sauce, as well as any Lot Code of Pretty Thai Sweet Chili Sauce are completely safe to consume. Product may be returned to H-E-B and/or Central Market for a full refund. Subsequent investigation indicates the problem was caused by a temporary breakdown in the manufacturer's production and packaging processes.
Consumers with questions may contact the Pretty Thai brand directly via email at info@ptfawg.com or via telephone at 512 981 6170. Consumers or retailers may also contact the manufacturer, Ponder Foods, via email at info@ponder-foods.com or via telephone at 469 914 0052 (M-F, 9:00am-5:00pm CDT).

Sunshine Mills, Inc. Issues Voluntary Recall of Certain Dog Food Products Due to Potentially Elevated Levels of Aflatoxin

September 2, 2020

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Sunshine Mills, Inc. is issuing a voluntary recall of certain dog food products due to levels of Aflatoxin that are potentially above the acceptable limit.  Aflatoxin is a naturally occurring mold by-product from the growth of Aspergillus flavus and can be harmful to pets if consumed in significant quantities.
The potential for aflatoxin levels above the acceptable limit in these products was discovered by routine sampling performed by the Louisiana Department of Agriculture and Forestry showing that a sample of a single 4-pound bag of one lot of the product contained elevated levels of aflatoxin.  No illnesses have been reported in association with these products to date, and no other Sunshine Mills, Inc. pet food products are affected by this announcement.
While no adverse health effects related to these products have been reported, Sunshine Mills, Inc. has chosen to issue a voluntary recall of these products as a precautionary measure in furtherance of its commitment to the safety and quality of its products.  Pets that have consumed any of the recalled products and exhibit symptoms of illness including sluggishness or lethargy combined with a reluctance to eat, vomiting, yellowish tint to the eyes or gums, or diarrhea should be seen by a veterinarian.
The affected products were distributed in retail stores nationally.  Retailers who received the recalled lots have been contacted and asked to pull these lots from their inventory and shelves.  There are no other Family Pet®, Heartland Farms®, or Paws Happy Life® products or other lot codes of these products affected by this precautionary recall.
Consumers who have purchased the recalled products should discontinue use of the product and may return the unused portion to the place of purchase for a full refund. Consumers may contact Sunshine Mills, Inc. Customer Service at (800) 705-2111 from 7AM to 4PM Central Time, Monday through Friday, or by email at customer.service@sunshinemills.com for additional information.
This is a voluntary recall being conducted in cooperation with the U.S. Food and Drug Administration.
Products affected by this announcement:
Product Name    Size    Lot Codes    UPC Code
FAMILY PET® MEATY CUTS BEEF CHICKEN & CHEESE FLAVORS PREMIUM DOG FOOD    4 lb.    TD3 4/APRIL/2020
TD1 5/APRIL/2020    3225120694
    14 lb.    
TB1 4/APRIL/2020
TB2 4/APRIL/2020
TB3 3/APRIL/2020    3225118078
    28 lb.    TB3 3/APRIL/2020    3225120694
HEARTLAND FARMS® GRILLED FAVORITES
BEEF CHICKEN & CHEESE FLAVOR    14 lb.    TB1 4/APRIL/2020
TB2 4/APRIL/2020    7015514299
    31 lb.    TA2 4/APRIL/2020
TA3 4/APRIL/2020    7015514301
PAWS HAPPY LIFE® BUTCHER’S CHOICE DOG FOOD    16 lb.    TA1 4/APRIL/2020
TA2 4/APRIL/2020    3680035763

Open Book Extracts Issues Voluntary Nationwide Recall of All Lots of Always Be Clean Hand Sanitizer and Just Hand Sanitizer that are Labeled to Contain Methanol

August 31, 2020

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Open Book Extracts (OBX) is voluntarily recalling to the consumer level all lots of Always Be Clean Hand Sanitizer and Just Hand Sanitizer that are labeled to contain methanol.
Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.
OBX sources hand sanitizer from a leading global chemical and ingredient distributor, and has verified through a third-party lab that the hand sanitizer does not contain reportable levels of methanol. The supplier updated the Safety Data Sheet (SDS) to remove methanol since it is below the reportable level, and we updated the labels accordingly.
These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available.
The mislabeled hand sanitizer was packaged in single-use packets and multi-count boxes using the following NDC and Lot codes:
Name of Product    NDC    Size    UPC    Lot
Always Be Clean hand sanitizer    75091-2020-1
75091-2020-2
75091-2020-3    Single snaps
100 Count
25 Count    375091202016
375091202023
375091202030    ES8-200514
Just Hand Sanitizer    78065-2020-1
78065-2020-2    Single Snaps
100 Count    703123998659
703123998598    ES9-200610
The mislabeled hand sanitizer was packaged from May 14, 2020 through June 1, 2020 and sold from May 15, 2020 through July 16, 2020 Nationwide in the USA to businesses for internal use.
OBX has notified all distributors via phone and email and is replacing all of the mislabeled product. While OBX believes that all mislabeled units have been recovered or, in the case of Just Hand Sanitizer, were relabeled prior to sale, anyone with questions regarding this recall or are in possession of Just Hand Sanitizer or Always Be Clean Hand Sanitizer from the above-listed lots that list methanol as an inactive ingredient may contact Open Book Extracts at handsanitizer@openbookextracts.com or 917-536-1194 (9 a.m.- 5 p.m. ET) to replace the hand sanitizer free of charge.
Distributors or businesses that have product labeled to contain methanol should stop distribution and return to place of purchase. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Ukrop's Homestyle Foods Recalls Chicken Salad Product Due to Misbranding and an Undeclared Allergen

August 31, 2020

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WASHINGTON, Aug. 31, 2020 – Ukrop’s Homestyle Foods, a Richmond, Va. establishment, is recalling approximately 1,202 pounds of ready-to-eat (RTE) chicken salad product due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product may contain almonds, a known allergen, which are not declared on the product label.
The RTE chicken salad item was produced on August 26, 2020. The following product is subject to recall: [View Labels (PDF only)]
•    15-oz. round plastic containers containing “Ukrop’s Chicken Salad” with a sell by date of “09/02/20”.
The product subject to recall bears establishment number “P-19979” inside the USDA mark of inspection. These items were shipped to retail locations in North Carolina, Ohio, Virginia, and West Virginia.
The problem was discovered after the firm received a consumer complaint reporting that the product contained almonds.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in retailer and consumers’ refrigerators. Retailers who have obtained these products are urged not to sell them. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Susan Rowe, Executive Administrator, Ukrop’s Homestyle Foods, at (804) 340-3050.

Harmonic Nature Issues Voluntary Nationwide Recall of Hand Sanitizer Due to the Presence of 1-Propanol

August 28, 2020

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Guadalupe, Nuevo Leon, Harmonic Nature is voluntarily recalling all 800 bottles Hand Sanitizer, 250mL, product due to the potential presence of 1-propanol. The products have been tested and found to contain 1 propanol.
Risk Statement: Any amount of 1-propanol with a concentration greater than or equal to 1% by volume that is unlisted in a product labeled as an ethanol-based hand sanitizer has a reasonable probability of acute toxicity from ingestion which can cause central nervous system depression, which could result in death, permanent impairment, or necessitate medical or surgical intervention. Populations most at risk include individual with alcohol addiction and adolescents, who have been known to ingest ethanol-based antiseptic rubs intentionally to become intoxicated, as well as infants and children who may unintentionally ingest the defective product. Harmonic Nature has not received any reports of adverse events related to this recall.
The product is used as a hand sanitizer and is packaged in 250 mL plastic bottles , with UPC Code 7500462892210. The product can be identified by Harmonic Nature as a hand sanitizer Topical Solution distributed only to and currently on hold at the US custom bróker, Aquiles INC.
Harmonic Nature is notifying Aquiles INC. and is arranging for return of all recalled product. Consumers with questions regarding this recall can contact Harmonic Nature by +(52) 8120 2967 03 or miguel_martinez2000@yahoo.com Monday to Friday from 8:00 am to 6:00pm central time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

B&G Foods Issues Voluntary Allergy Alert on Undeclared Milk in a Limited Number of Boxes of Back to Nature® Organic Rosemary & Olive Oil Stoneground Wheat Crackers

August 26, 2020

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B&G Foods announced today it is voluntarily recalling 1,502 cases of a single date code of 6 oz. Back to Nature Organic Rosemary & Olive Oil Stoneground Wheat Crackers, with a “best by” date of APR 07 2021, after learning that the product may contain undeclared milk ingredients. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume the product contained in the recalled boxes. There is no health risk associated with this product for individuals without an allergy to milk.
This recall affects only 1,502 cases of the following product, which were distributed in retail stores nationwide:
Description    Consumer UPC #    Size    Best By Date
Back to Nature Organic Rosemary & Olive Oil Stoneground Wheat Crackers    8-19898-01015-8    6 oz.    APR 07 2021
(The “best by" date is located on the top of the box.)
This recall does not apply to any other “best by” dates, sizes or varieties of Back to Nature products.
No allergic reactions related to this matter have been reported to date. This recall was initiated in cooperation with the FDA and the third party co-packer that produced the product.
B&G Foods discovered this issue when it received a consumer complaint that the foil bag within a single box of Back to Nature Organic Rosemary & Olive Oil Stoneground Wheat Crackers contained cheese crackers. B&G Foods initiated the recall based on the results of its investigation after locating a second box in its warehouse with the same “best by” date that was inadvertently filled with a foil bag of cheese crackers, potentially exposing consumers to undeclared milk. The foil bags do correctly indicate whether the crackers are rosemary & olive oil crackers or cheese crackers and the outer box provides an allergen advisory statement indicating that the product is “Made on the same equipment that processes milk.” However, out of an abundance of caution, B&G Foods is recalling all 1,502 cases with this particular “best by” date that have been shipped to its customers. Product with this particular “best by” date was shipped and distributed by B&G Foods to its customers' warehouses located in Arizona, California, Colorado, Georgia, Iowa, Maryland, Missouri, New Jersey, New York, Tennessee, Washington and Wisconsin.
Consumers who have purchased the recalled products can return them to the place of purchase for a full refund. Consumers seeking a refund or additional information may also contact B&G Foods by calling 855.346.2225 Monday through Friday from 8:30 a.m. to 6:00 p.m. Eastern time or submitting a contact at https://backtonaturefoods.com/contact-usExternal Link Disclaimer.

Nanomateriales, Sa De CV Issues Voluntary Nationwide Recall of All Lots of Zanilast+gel Due to the Presence of 1-Propanol

August 26, 2020

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Apodaca, Nuevo Leon, Nanomateriales is voluntarily recalling all lots of ZANILAST+ GEL, Sanitizer gel, to the consumer level. FDA laboratory analysis found ZANILAST+ GEL to contain 1-propanol.
Risk Statement: There is a reasonable probability of acute toxicity from ingestion which can cause central nervous system depression, which could result in death, permanent impairment, or necessitate medical or surgical intervention. Populations most at risk include individual with alcohol addiction and adolescents, who have been known to ingest ethanol-based antiseptic rubs intentionally to become intoxicated, as well as infants and children who may unintentionally ingest the defective product. Nanomateriales, SA de CV has not received any reports of adverse events related to this recall.
The product is used as a sanitizer gel, for hand washing to decrease bacteria on the skin and is packaged in 1 liter, 25 liters, and 1 gallon plastic bottles distributed from 05/29/2020 to 06/17/2020 in the States of California, New York and New Jersey.
Presentation    UPC    NDC    Lable
1 Liter    2 000000 531151    69912-008-01    See below
25 Liter    2 000000 531151    69912-006-01    See below
1 galon    2 000000 531144    69912-008-02    See below
Nanomateriales, SA de CV is notifying its distributors and customers by e-mail and phone and is arranging for return of all recalled products. Consumers and distributors that have ZANILAST+ GEL which is being recalled should return to place of purchase.
Consumers with questions regarding this recall can contact Nanomateriales SA de CV by phone (+1 (210)963 5679) or e-mail (contacto@nanomateriales.com.mx) on working days (Monday through Friday) from 10:00 AM to 5:00 PM, Central Time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Riviana Foods Inc. Voluntarily Recalls Certain Manufacturing Date and Upc Number of Ronzoni® Smart Taste® Extra-Wide Noodles Due to Possible Undeclared Egg Allergen

August 26, 2020

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Riviana Foods Inc. is voluntarily recalling 19,931 cases of certain coded Ronzoni Smart Taste Extra-Wide Noodle cellophane packages that contain an egg noodle product. The affected Ronzoni Smart Taste Extra-Wide Noodle packages do not declare the allergen “egg”, which is an ingredient in the noodle product. People who have an allergy or severe sensitivity to egg run the risk of serious allergic reaction if they consume this product. The affected product was distributed nationally from March through August of this year.
The product at issue can be identified by the manufacturing code and UPC number listed on the package as listed in the chart below.
Product Size    Product Name    Manufacturing Codes    Individual Package UPC
12 oz. each    RONZONI® Smart Taste® Extra-Wide Noodles    MAR3022H, MAR3122H, JUN0422H, JUN0522H, JUL2422H, JUL2522H    71300 05008
No other varieties and no other manufacturing codes are included in this recall.
At this time, Riviana has received one consumer complaint and no reports of illness or injury associated with this product.
The recall was initiated after it was discovered that product containing egg was distributed in packaging that did not reveal the presence of egg. Subsequent investigation indicates the problem was caused by a temporary breakdown in Riviana’s packaging review processes.
Riviana has instructed distributors and retailers who purchased affected product from Riviana to segregate the recalled products from their inventories so that a Riviana sales representative may assist retailers in the disposition of the product.
Consumers should return the affected product to the store where they purchased it for a full refund. Consumers who may have questions or concerns should call Riviana’s toll free Consumer Relations number at 1-800-730-5957, Monday through Friday, between 9 am and 5 pm (Eastern).

Schaws Sauce Issues Allergy Alert on Undeclared Soy and Anchovies in Schaws Sweet and Sassy Gourmet Barbecue and Basting Sajuce and Schaws Sweet with Heat Barbecue and Basting Sauce

August 26, 2020

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Schaws Sauce of Iron River, Michigan is recalling two flavors of barbeque sauces, because the products contain undeclared Soy and Anchovies. People who have an allergy or severe sensitivity to Soy or Anchovies run the risk of serious life threatening allergic reaction if they consume these products.
Schaws Sauce is distributed primarily in Michigan, but it is also retailed through the company web site, schaws sauce.com. The two affected flavors are: Schaws Sweet and Sassy Barbecue and Basting Sauce and Schaws Sweet with Heat Barbecue and Basting Sauce. Both are sold in clear 18 oz. jars with white metal lids. All jars with a use by date of 8/20/2022 and prior are impacted by this recall.
No illnesses have ever been reported to date in connection with this problem.
This announcement was initiated after the omission on the label was discovered August 20 of this year during a routine operations inspection. This inspection revealed that two ingredients, soy and anchovies (fish), were used in the brand of Worcestershire sauce used in the production of Schaws Sauce.
Individuals with an allergy or sensitivity to Soy or Anchovies should not consume these products. Households that include individuals with an allergy or sensitivity to either of these allergens should dispose of the recalled product. Customers who have purchased Schaws BBQ Sauce in either the original or thew/heat variety and have allergy to either fish products or soy, may return the bottle to Schaws Sauce, 176 Stanley Lake Drive, Iron River, Michigan 49935 and have their money refunded by calling 1-800-797-5226 between the hours of 9:00 A. M. and 4:00 P. M. central time Monday thru Friday.

Russ Davis Wholesale Recalls Peaches and Peach Salsa Because of Possible Health Risk

August 25, 2020

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Russ Davis Wholesale (RDW) is recalling Peach Salsa under the Crazy Fresh and Quick & Easy brands in an abundance of caution due to possible contamination with Salmonella.
Salmonella may cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
This recall is in response to Wawona Packaging initiating a recall of peaches early in the day August 22, 2020 as an ingredient provider to Russ Davis Wholesale.
To date, Russ Davis Wholesale has not received any reported illnesses related to this organism.
The affected products are:
UPC    Product Name    Brand Name on Label    Packaging    Image    SELL BY Date
795631 820270    Crazy Fresh Perfectly Peach Salsa    Crazy Fresh Perfectly Peach Salsa    8 oz.    See below    6/25/2020 to 8/26/2020
795631 820270    Quick & Easy Perfectly Peach Salsa    Quick & Easy Perfectly Peach Salsa    8 oz.    See below    7/29/2020 to 8/26/2020
795631 820270    Clear Label Perfectly Peach Salsa    Clear Label Perfectly Peach Salsa    8 oz.    See below    7/30/2020 to 8/23/2020
Affected product was delivered to retail stores in Minnesota, Wisconsin, North Dakota, South Dakota, Michigan, Iowa, Nebraska, and Wyoming.
Some containers of peach salsa may have been purchased from the deli counter at grocery stores located in Ortonville, MN, Cross Lake, MN and Tipton, IA.
Five Bountiful Fresh gift baskets, also containing the recalled peaches were sold through one location in Hastings, MN.
Retailers have been instructed to remove affected products from store shelves and destroy.
Consumers are urged to immediately throw any product they may have away and not consume.
Consumers with questions may contact the company at: customerservice@russdaviswholesale.com or 877-433-2173 between 8:00 am and 5:00pm central standard time.

Asiaticon SA de CV Issues Voluntary Nationwide Recall of V-Klean Hand Sanitizer Gel, Medically Minded Hand Sanitizer Gel and Protz Real Protection Antibacterial Hand Sanitizer Due to Potential Presence of Methanol (Wood Alcohol) and Subpotent Ethanol Levels

August 25, 2020

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Mexico City, Mexico, Asiaticon SA de CV (Mexico) is voluntarily recalling all lots of V-Klean Hand Sanitizer Gel, Medically Minded Hand Sanitizer Gel and Protz Real Protection Antibacterial Hand Sanitizer sold in 13.5, 16.9 and 33.8 ounce bottles to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol) and subpotent ethanol levels.
Risk Statement:  Methanol has inferior antiseptic properties compared to ethanol.  Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death.  Although all person using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date Asiaticon SA de CV has not received reports of adverse events related to this recall.
The product is used as a hand sanitizer and is packaged in plastic clear bottles with clear tops with UPC Code:
V-Klean in 8.5 fl. oz. (250 ml) bottles: 716053704993
V-Klean in 16.9 fl. oz. (500 ml) bottles: 716053704993
V-Klean in 33.8 fl. oz. (1000 ml) bottles: 716053704993
Medically Minded in 16.9 fl. oz. (500 ml) bottles: 676753003782
Protz in 13.5 fl. oz. (400 ml) bottles : 7503019005002
The recall includes all lots.  This product was exported to different distributors nationwide.
Asiaticon SA de CV is notifying its distributors by voluntary recall letter and consumers via this press release. Consumers that have the product subject to this recall should stop using and either contact Asiaticon SA de CV per the below for disposal instructions or return it to the place of purchase.
Consumers with questions regarding this recall can contact Asiaticon SA de CV at direccion@asiatic-connection.com (0052 1 55 21553488).  In the US: at 929 394 3020 (available Monday to Friday 9.30 am  6 pm eastern time) Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Hostess Brands, LLC Expands Voluntary Recall of Certain Hostess® Raspberry Zingers® Due to the Potential for Mold

August 25, 2020

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Hostess Brands, LLC (“Hostess Brands”) is expanding its voluntary recall of certain Hostess® Raspberry Zingers® because the product may develop mold prior to the best by date.
The expanded recall applies to the following Raspberry Zinger® products:
Product Description:    Item UPC:    Batch:    Best By Dates:
Hostess Raspberry Zingers (Multi-Pack fresh)    888109110604    H062424000 H062524000 H062624000 H062724000 H070724000 H070824000 H070924000 H071024000 H071124000 H072124000 H072224000 H072324000    09/07/2020 09/08/2020 09/09/2020 09/10/2020 09/20/2020 09/21/2020 09/22/2020 09/23/2020 09/24/2020 10/04/2020 10/05/2020 10/06/2020
Hostess Raspberry Zingers (Multi-Pack frozen)    888109110604    H062624000 H062724000    N/A N/A
Hostess Raspberry Zingers (Single-Serve fresh)    888109010089    H062424000 H062624000 H070724000 H070824000 H072224000 H072324000    09/07/2020 09/09/2020 09/20/2020 09/21/2020 10/05/2020 10/06/2020
Hostess Raspberry Zingers (Single-Serve frozen)    888109010089    H062424000 H062524000 H062624000 H070824000 H070924000 H072124000 H072224000    N/A N/A N/A N/A N/A N/A N/A
Hostess Raspberry Zingers (Single-Serve 3 count case)    888109010089    H062424000 H062624000 H071124000 H072324000    09/07/2020 09/09/2020 09/24/2020 10/06/2020
The following Raspberry Zinger® products were part of the original voluntary recall:
Product    Item UPC    Batch    Best By Date
Hostess Raspberry Zingers (Multi-Pack fresh)    888109110604    H061224000    08/26/2020
        H061324000    08/27/2020
        H061424000    08/28/2020
        H061524000    08/29/2020
Hostess Raspberry Zingers (Multi-Pack frozen)    888109110604    H061524000     
Hostess Raspberry Zingers (Single-Serve fresh)    888109010089    H061224000    08/26/2020
        H061324000    08/27/2020
        H061424000    08/28/2020
Hostess Raspberry Zingers (Single-Serve frozen)    888109010089    H061424000     
        H061524000     
Hostess Raspberry Zingers (Single-Serve grocery 3 count)    888109010089    H061224000    8/26/2020
The products were sold to mass merchandisers, grocery stores, distributors, dollar and discount stores, and convenience stores throughout the United States.
Consumers who have purchased the affected product are urged to discontinue consumption and contact the place of purchase about returning them for a full refund.
This recall does not affect any other Hostess Brands products.
Consumers with questions may contact 1-800-483-7253 Monday through Friday from 8:30 am to 4:30 pm Central Time.

Sunshine Mills, Inc. Issues Voluntary Recall of Nature’s Menu® Super Premium Dog Food with a Blend of Real Chicken & Quail Because of Possible Salmonella Health Risk

August 24, 2020

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Sunshine Mills, Inc. is issuing a voluntary recall of Nature’s Menu® Super Premium Dog Food with a Blend of Real Chicken & Quail because of the potential to be contaminated with Salmonella. Salmonella can affect animals eating the products and there is risk to humans from handling contaminated products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.
Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.
Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.
The recalled products were distributed in retail stores nationally and can be identified with the following UPC 7015514363 and UPC 7015514365.
The product comes in a 3-pound bag with the following lot codes:
TE1 20/April /2020, TE1 21/April/2020, TE1 22/April/2020, TE2 20/April /2020, TE2 21/April/2020,
TE2 22/April/2020, TE3 20/April/2020, TE3 21/April/2020, TE3 22/April/2020.
The product comes in a 13.5-pound bag with the following lot codes:
TB1 20/April /2020, TB1 21/April/2020, TB1 22/April/2020, TB2 20/April /2020, TB2 21/April/2020,
TB2 22/April/2020, TB3 20/April/2020, TB3 21/April/2020, TB3 22/April/2020.
There are no other Nature’s Menu® products or other lot codes of the Nature’s Menu® Super Premium Dog Food with a Blend of Real Chicken & Quail affected by this precautionary recall.
No illnesses, injuries or complaints have been reported to date.
The potential for contamination was noted after the firm was notified by the Georgia Department of Agriculture when a sample of a single 3-pound bag of the product was collected and tested positive for Salmonella.  The firm conducted testing of multiple samples of the same lot which all tested negative for Salmonella. Salmonellamay not be evenly distributed throughout a lot which is why it could have been found on one sample and not on multiple other samples of the same lot.  However, out of an abundance of caution, Sunshine Mills, Inc. has chosen to issue a voluntary recall of the above-referenced lots of Nature’s Menu® Super Premium Dog Food with a Blend of Real Chicken & Quail in furtherance of its commitment to the safety and quality of its products.
Retailers who received the recalled lots have been contacted and asked to pull these lots from their inventory and shelves.  Consumers who have purchased Nature’s Menu® Super Premium Dog Food with a Blend of Real Chicken & Quail from the recalled lots should discontinue use of the product and may return the unused portion to the place of purchase for a full refund. Consumers may contact Sunshine Mills, Inc. customer service at (800) 705-2111 from 7AM to 4PM Central Time, Monday through Friday, or by email at customer.service@sunshinemills.com for additional information.
This is a voluntary recall being conducted in cooperation with the U.S. Food and Drug Administration.

Oberto Snacks, Inc. Recalls Smoked Sausage Products Due to Misbranding and an Undeclared Allergen

August 22, 2020

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WASHINGTON, Aug. 22, 2020 – Oberto Snacks Inc., a Kent, Wash. establishment, is recalling approximately 309 pounds of smoked sausage products due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains soy, a known allergen, which is not declared on the product label.
The smoked sausage items were produced on March 21, 2020. The following product is subject to recall:
•    3-oz. flexible plastic packages containing “CATTLEMAN’S CUT SMOKED SAUSAGES OLD FASHIONED” with a “BEST BY 21MAR2021 22” date and a time range between 18:35 to 19:15.
The products subject to recall bear establishment number “EST. 2862B” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.
The problem was discovered on Aug. 21, 2020 after the firm was informed by its distributor that a product from Oberto Snacks Inc. displayed the incorrect nutrition and ingredients label, which did not list soy as an ingredient.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Members of the media with questions about the recall can contact Marc Berger, Nyhus Communications, at (402) 730-5666. Consumers with questions about the recall can contact Stephanie Larson, Oberto Snacks Inc., Senior Sales Support Manager, at (253) 437-6330.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Prima® Wawona Recalls Bagged Peaches Due to Possible Salmonella Risk

August 21, 2020

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Prima® Wawona of Fresno, California is voluntarily recalling its Wawona, Wawona Organic brand conventional and organic bagged peaches because the product could possibly be contaminated with Salmonella.
Salmonella is a microorganism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
Peaches sold as loose fruit or in bulk are not associated with this recall. Only bagged peaches are included in this recall.
The peaches were distributed and sold from June 1st to August 19th in supermarkets with the following product codes:
Wawona Peaches – 033383322001
Wawona Organic Peaches – 849315000400
Prima® Peaches – 766342325903
Organic Marketside Peaches – 849315000400
Kroger Peaches – 011110181749
Wegmans Peaches – 077890490488
The product codes may be found at the bottom of each package.
The bagged peaches were distributed through retailers in the following states: Alaska, Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Minnesota, Missouri, Mississippi, North Carolina, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia and Wisconsin.
Prima® Wawona is recalling the bagged peaches as a precaution in connection with a Salmonella outbreak under investigation by the U.S. Food and Drug Administration and the U.S. Centers for Disease Control and Prevention that is suspected to have caused the illness of more than 60 people in nine states.
“We’re conducting this voluntary recall in cooperation with the FDA out of consideration for the wellbeing and safety of our customers and consumers,” said George Nikolich, Vice President Technical Operations. “We continue to be committed to serving consumers with high quality fruit.”
Anyone who has the recalled product in their possession should dispose of it immediately or return it to the place of purchase for a refund. Consumers with questions may contact Prima Wawona’s toll-free number at 1-877-722-7554, from 8 a.m. to 5 p.m. ET, Monday through Friday, or visit its website at wawonapacking.comExternal Link Disclaimer.

Superior Nut Company Issues Allergy Alert on Undeclared Brazil Nuts in Product

August 20, 2020

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Superior Nut Company of Cambridge, MA is recalling Southern Grove Mixed Nuts Less than 50% Peanuts, because it may contain undeclared Brazil Nuts. People who have an allergy or severe sensitivity to Brazil nuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Product was distributed by select Aldi stores in Connecticut, Massachusetts, New Hampshire, New York, Ohio, Pennsylvania, Rhode Island and Vermont.
The product is packed in 14.75 oz. cans under Southern Grove brand, Mixed Nuts 50% Peanuts Lot Codes 0MR105975; 0MR106051; 0MR106280; 0MR106320.
No illnesses have been reported to date.
The recall was initiated after it was discovered that product containing Brazil Nuts was distributed in packaging that did not reveal the presence of Brazil Nuts.
Consumers who have purchased the product are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-251-6060, Monday to Friday 9AM to 4:00PM
Superior Nut Company, Inc.
225 Monsignor O’Brien Hwy
Cambridge, MA 02141

Mexico Sa De CV Issues Voluntary Nationwide Recall of All Lots of Florence Morris Antiseptic Hand Sanitizer Due to Presence of Methanol (Wood Alcohol) and Sub-Potent Ethanol

August 20, 2020

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Grupo Asimex De Grupo Asimex de Mexico SA de CV is voluntarily recalling all lots of FLORANCE MORRIS Antiseptic Hand Sanitizer, 70% Alcohol, packaged in 8 fl oz bottles and 1L bottles to the consumer level. The products have the potential to contain methanol (wood alcohol) and be sub-potent for the ethanol content.
Risk Statement: The use of sub-potent hand sanitizer products can have adverse health consequences related to infections. Ethanol levels below the label claim can result in a lack of efficacy. In addition, methanol has inferior antiseptic properties compared to ethanol. Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all person using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, Grupo Asimex de Mexico SA de CV has not received reports of adverse events related to this recall.
Recalled Products: These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. The recalled products are as follows:
Product, Sizes and LOT:
FLORANCE MORRIS Antiseptic Hand Sanitizer
8 fl oz, 1 L
LOT CODES: 200520673, 200520674, 200525677, 200601685
The Hand Sanitizer is packaged in an 8 oz. and 1L plastic clear bottles with flip-top caps. Product was distributed in the state of FLORIDA in the United States through one distributor.
Grupo Asimex de Mexico is notifying its distributor by recall letter and consumers via this press release. Grupo Asimex de Mexico is arranging for the return and refund of all recalled products. Consumers/distributors that have the product subject to this recall should stop using/ distributing/ selling the Hand Sanitizer and return it to the place of purchase.
Consumers with questions regarding this recall can contact Grupo Asimex de Mexico SA de CV during business hours to the following email: sales@asimexglobal.com Event: Recall
Consumers should contact their physician or healthcare provider if they experienced any problems that may be related to the use of this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Allergy Alert for Undeclared Soy (Soy Milk) in Vegan Vanilla Cake Issued by Whole Foods Market Stores in Seven States

August 20, 2020

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Whole Foods Market is voluntarily recalling Vegan Vanilla Cake from 21 stores across Alabama, Georgia, Mississippi, North Carolina, South Carolina, Tennessee and one store in Tallahassee, Florida, due to an undeclared soy (soy milk) allergen. People who have a food allergy or severe sensitivity to soy run the risk of serious or lifethreatening allergic reaction if they consume this product.
The affected product was sold as whole, 6-inch cakes in both the cake case and self-serve areas of the Bakery Department. The product was packaged in plastic dome containers with Whole Foods Market scale labels, a PLU code of 41070 and product sell-by date through August 24, 2020. All affected product has been removed from store shelves. 
No allergic reactions have been reported to date. The recall was initiated when a Team Member conducting a labeling audit identified the missing ingredient.
Customers who purchased this product at Whole Foods Market can bring a valid receipt into stores for a full refund. Consumers with additional questions can call 1-844-936-8255 between the hours of 7:00 a.m. and 10:00 p.m. CST, Monday through Friday, or 8:00 a.m. and 6:00 p.m. Saturday through Sunday.

ALDI Voluntarily Recalls Assorted Peaches from Wawona Packing Company LLC Due to Possible Salmonella Enteritidis Contamination

August 19, 2020

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As a precautionary measure, ALDI is voluntarily recalling assorted peaches received from its supplier, Wawona Packing Company, due to possible Salmonella contamination.
ALDI has removed the affected peaches from select ALDI stores in Connecticut, Florida, Illinois, Iowa, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, North Dakota, New Hampshire, New York, Ohio, Pennsylvania, Rhode Island, South Dakota, Vermont, Virginia, Wisconsin and West Virginia. The items were also available for purchase through the company’s partnership with Instacart, a grocery delivery service.
The affected products and UPC codes can be found below:
Product    Packaging    UPC Code    Select Stores in These Affected States
Wawona Peaches 2 lb.    2 lb. bag    033383322001    Connecticut, Florida, Illinois, Iowa, Kentucky, Maryland, Massachusetts, Michigan, Minnesota, North Dakota, New Hampshire, New York, Ohio, Pennsylvania, Rhode Island, South Dakota, Vermont, Virginia, Wisconsin and West Virginia
Loose Bulk Peaches    Loose Bulk    N/A    Connecticut, Florida, Illinois, Iowa, Kentucky, Massachusetts, Michigan, Minnesota, North Dakota, New Hampshire, New York, Ohio, Rhode Island, South Dakota, Vermont, Wisconsin and West Virginia
Peaches Organic 2 lb.    2 lb. bag    849315000400    Connecticut, Illinois, Iowa, Massachusetts, Michigan, Minnesota, North Dakota, New Hampshire, New York, Ohio, Pennsylvania, Rhode Island, South Dakota, Vermont, Wisconsin and West Virginia
ALDI takes the safety and integrity of the products it sells seriously. If customers have product affected by this voluntary recall, they should discard it immediately or return it to their local store for a full refund.
Customers with additional questions can contact Wawona Packing Company LLC Customer Service at 1-877-722-7554.
ALDI sincerely regrets any inconvenience and concern this voluntary recall may cause.
About ALDI U.S.
One of America's fastest growing retailers, ALDI operates nearly 2,000 stores across 36 states. Since 1976, ALDI has offered a unique shopping experience that is designed to save customers money on the groceries they want most while never having to compromise on quality or selection. For more information about ALDI, visit aldi.us.

Maison Terre Issues Voluntary Nationwide Recall of Organic Goldenseal Root Powder Due to Microbial Contamination

August 19, 2020

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North Little Rock, AR, Maison Terre is voluntarily recalling all lots of its Goldenseal Root Powder, purchased from Starwest Botanicals, Sacramento, CA, and repackaged to the consumer level due to microbial contamination. FDA laboratory analysis of product samples found these products to be contaminated with various microorganisms including: Enterobacter cloacae, Cronobacter sakazakii, Cronobacter dublinensis, among others.
Risk Statement: The use of contaminated product in otherwise healthy patients can result in infections necessitating antimicrobial and potentially surgical treatment. In individuals with weak immune systems and infants, the use of the product can result in death. Maison Terre has received a report of one infant death associated with use of this product on the umbilical cord stump.
The product is a yellow colored powder that comes in a clear plastic bag, net weight of 1 oz.
The recalled Goldenseal Root Powder was distributed nationwide in the USA to customers who ordered through Amazon.com and purchased between the dates of 01/25/2015 to 08/04/2020.
Maison Terre is notifying its customers by email through Amazon.com. Customers who have purchased the Goldenseal Root Powder are urged not to consume or apply it. Customers are urged to dispose of any unused portion. For those customers wanting to return the product for a refund, please contact Maison Terre for a return shipping label.
Customers with questions regarding this recall may contact Maison Terre at 501-888-9438, Mon-Fri, 10 am - 4 pm CST or at info@maisonterre.net. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
Maison Terre is conducting this recall with the knowledge of the U.S. Food and Drug Administration.

Albek de Mexico S.A. de C.V. Issues Voluntary Nationwide Recall of All Hand Sanitizers Due to Potential Presence of Undeclared Methanol

August 19, 2020

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SAN JUAN del RIO QUERETARO, Mexico -- ALBEK de Mexico S.A. de C.V. is voluntarily recalling all lots and all brands of hand sanitizer currently in US distribution to the consumer level. The products were manufactured between November 7, 2019 and June 28, 2020.
This recall is being initiated out of an abundance of caution due to detection of methanol in hand sanitizer samples manufactured by Albek when product was presented for import into the United States.
Risk Statement: Substantial methanol exposure could result in serious health effects (including nausea, diarrhea, vomiting, severe abdominal pain, headache, blurred vision, permanent blindness, seizures, coma, nervous system damage) or death. Persons using methanol-based products on their hands may be at risk. Young children who accidently ingest them and adolescents and adults who drink such products are most at risk for methanol poisoning. To date, there have been no reports of serious adverse events related to the products in the scope of this recall.
Recalled Products: The products are labeled for use as a hand sanitizer (or “antiseptic”) and are packaged for several nationwide distributors in a variety of formats as indicated in the table as follows:
BRANDS:    Nuuxsan    Modesa    Assured    Assured    Next
Product Name    Nuuxsan Instant Hand Sanitizer    Modesa Hand Sanitizer with Moisturizers and Aloe Vera    Assured Hand Sanitizer Vitamin E and Aloe    Assured Hand Sanitizer Aloe Vera    Next Hand Sanitizer
NDC    72758-005-02, 72758-001-08    72758-011-23    72758-010-23    72758-009-23    50066-605-08
Sizes    8 fl oz    8 fl oz    8 fl oz    8 fl oz    8 fl oz
UPC    713620000175    32251380426    639277928597    639277928610    650240053573
Affected Lots    All Lot #s    1931104AL    1931101AL    1931102AL    The affected lots end in:
1001, 1002, 1003, 1004, 1005
These products were distributed nationwide in the United States beginning on November, 15 2019.
Albek is partnering with its distributors, who will help notify their customers by phone calls, emails, and/or mailed letters and is arranging for return of all recalled products. Consumers, distributors, and retailers that have product which is being recalled should stop use or distribution and return to place of purchase.
Consumers with questions regarding this recall can contact Albek de Mexico S.A. de C.V. during the business hours business hours: 9:00am – 5:00pm (CT)
Email: contact@albek.com.mx
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using these products.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

HelloFresh Urgent Onion Recall Notification

August 19, 2020

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HelloFresh has been informed by one of its ingredient suppliers that it is conducting a voluntary recall of its onions due to the potential presence of salmonella bacteria. Please discard all onions received from May 8 through July 31, 2020.
We recommend disposing of all onions received during the specified time period. For further information on whether you have been impacted, please check the product codes, located on the bottom square of your box shipping label. Please see the photo provided below as reference for locating the product code.
Production Week    Production Week Start Date    HelloFresh Product Codes*
*Number sequence may vary    Everyplate Product Codes*
*Number sequence may vary
20    5/08    2-3-5-6-17    81-82-84-86-92-94
21    5/15    2-8-15-19    82-86-83-93
22    5/22    2-5-6-9-20    87-88-89-93-90-94
23    5/29    6-8-9-15-B- 3-5-20    82-84-86-87-89-91-92-95
24    6/5    6-8-17- B    82-84-86-89-90-95-83-93
25    6/12    3-4-10-15-18-17-19-20    82-87-88-95-82-87-88-95
26    6/19    2-3- 8-12    88-89-84-93
27    6/26    5-17- 4-15-18-20    82-87-89-90-91- 84-92-93
28    7/3    3-9-10-12-15-17- 6    85-86-90-91
29    7/10    3-20-7-21    82-88-89-90-92-96
30    7/17    4-19-21    82-84-89-94-96- 83-95
31    7/24    2-3-4-19-7-8-16    82-92- 81-84-87-89-94-96-98
As noted above, customers should immediately discard all onions received. We also recommend extra caution in disinfecting and sanitizing surfaces and containers that may have come in direct contact with these products, as recommended by the FDA. In the event that the onions have been consumed, please note that thoroughly cooking the product to 165ºF/74ºC, as instructed by the recipe, will kill the salmonella bacteria.
If you are experiencing any symptoms, including but not limited to, fever, diarrhea, or nausea, please contact your healthcare provider immediately. Click here for more information from the FDA about this supplier recall and the potentially related symptoms.
We sincerely apologize for this supplier-related incident. Your safety is our highest priority and we have taken immediate steps to ensure our onions are no longer sourced from this supplier. All HelloFresh facilities are SQF (Safe Quality Food) certified, which is the highest level of food safety certification and our teams follow a rigorous process to maintain the safety and quality of our meal kits. If you have any additional questions, please contact HelloFresh at hello@hellofresh.com.

Faribault Foods Inc. Recalls Canned Soup Product Due to Misbranding and Undeclared Allergens

August 19, 2020

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WASHINGTON, Aug. 18, 2020 – Faribault Foods Inc., a Faribault, Minn. establishment, is recalling approximately 15,134 pounds of canned soup product due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains milk and soy, known allergens, as well as beef and pork, which are not declared on the product label.
The cans labeled as chicken noodle soup actually contain a meatball and pasta product. The canned soup items were produced on May 26, 2020. The following products are subject to recall: [View Labels (PDF only)]
•    14-oz. cans of “PROGRESSO ORGANIC CHICKEN NOODLE SOUP” with a best by date of “BestByMAY262022” printed on the bottom of the can and a best by date of “09JUN2022” printed on the product case.  
The products subject to recall bear establishment number “EST18826A” printed on the bottom of the can under the best by date. These items were shipped to retail locations nationwide.
The problem was discovered when the firm’s distributor notified FSIS of consumer complaints that the soup contained meatballs and pasta instead of chicken and noodles.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Members of the media with questions about the recall can contact the General Mills Media Help Line at 763-764-6364 or Media.line@genmills.com. Consumers with questions about the recall can contact the General Mills Consumer Help Line at 1-800-200-9377.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

SG24 LLC Issues Voluntary Nationwide Recall of SkinGuard24 Hand Sanitizer Labeled to Contain Methanol

August 15, 2020

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SG24 LLC is voluntarily recalling the SkinGuard24 – All Day Hand Sanitizer products listed below to the consumer level. These products are being recalled because they are labeled to contain methanol.
Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, SG24 LLC. has not received any reports of adverse events related to the products of this recall.
Product Name    Size    UPC    SKU
SkinGuard24 – All Day Hand Sanitizer Plastic bottle with Foam Pump    8 oz (250 mL)    7 93573 147125    051230024
SkinGuard24 – All Day Hand Sanitizer Plastic bottle with Foam Pump    2.67 oz (70 ml)    7 93573 147103    051220024
SkinGuard24 – All Day Hand Sanitizer Spray Pocket Pen    10 mL    7 93573 14709    051210048
SkinGuard24 – All Day Hand Sanitizer Individual Towelette packaged as Single Use    2.5 x 3.75         03150025
The recalled products are used as a hand sanitizer for hand washing to decrease bacteria on the skin when soap and water are not available. The recalled products are packaged in PET or High-density polyethylene (HDPE) plastic bottle or pen and as Individually packaged Towelettes with UPC’s 7935733144725, 79357314703, 7935733147103, 79357314709. The recalled products label colors are teal and blue which includes the words SkinGuard24- All Day Hand Sanitizer. The recalled products were distributed nationwide throughout the United States.
SG24 LLC is notifying its customers/distributors by recall letter and consumers via this press release. We are also notifying our distributors, who will help notify their customers by phone calls, emails, and/or mailed letters and is arranging for return of all Recalled Products.
Consumers, distributors, and retailers that have recalled products should stop use or distribution and return to place of purchase. Consumers should contact their physician or healthcare provider if they experience any of the aforementioned problems that may be related to the use of this product.
Consumers with questions regarding this recall can contact SG24 LLC 1.877.470.8618 Ext. 20, Mon-Fri during business hours 9:00 AM - 4:30 PM (EST) or e-mail to recall@skinguard24.com or recall@sg24llc.com.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Company Contact Information
SG24 LLC
P O Box 406
Bolingbroke, GA 31004
Ph: 1.877.470.8618

Kroger Recalls Cheese Dips Because of Possible Health Risk

August 12, 2020

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Kroger is recalling cheese dips sold at because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. No customer illnesses have been confirmed to date.
On July 31, the company was notified by supplier Onions 52 that it had received red, yellow, and white onions from Thomson International, Inc., which had been implicated in the salmonella-related outbreak. On August 1, bulk onions sourced from Thomson International, Inc. were removed from sale in stores that had been identified as receiving the affected product. Subsequently, it was determined that several in-store made cheese dips may have used red onions from the produce department as an ingredient.
The dips, which are in plastic containers, were sold between May 15, 2020 and August 6, 2020. Items impacted include:
Product    UPC
MURRAY’S CHADS SMOKED GOUDA DIP    207083-00000
MURRAY’S JALEPENO JARLSBERG DIP    207181-00000
MURRAY’S BACON CHIVE JARLSBERG DIP    207182-00000
MURRAY’S SOUTHWESTERN JARLSBERG DIP    207185-00000
JARLSBERG DIP    207201-00000
JARLSBERG CHEESE SPREAD    216407-20000
PIMENTO CHEESE DIP    226481-60000
DELI JARLSBERG JALAPENO DIP    236293-70000
DELI BACON CHIVE JARLSBERG DIP    236294-70000
DELI SOUTHWESTERN JARLSBERG DIP    236295-70000
DELI JARLSBERG DIP    237462-40000
JARLSBERG DIP    247199-00000
DELI JARLSBERG CHEESE DIP    286292-70000
DELI APPLEWOOD CHEDDAR DIP    286462-20000
DELI BUFFALO BLUE CHEESE SPREAD    295095-50000
DELI SOUTHWEST CHEESE SPREAD    295408-50000
DELI RANCH CHEESE SPREAD    295409-50000
MURRAY’S CHADS SMOKED GOUDA DIP    207083-00000
MURRAY’S JALEPENO JARLSBERG DIP    207181-00000
MURRAY’S BACON CHIVE JARLSBERG DIP    207182-00000
MURRAY’S SOUTHWESTERN JARLSBERG DIP    207185-00000
JARLSBERG DIP    207201-00000
JARLSBERG CHEESE SPREAD    216407-20000
PIMENTO CHEESE DIP    226481-60000
DELI JARLSBERG JALAPENO DIP    236293-70000
DELI BACON CHIVE JARLSBERG DIP    236294-70000
DELI SOUTHWESTERN JARLSBERG DIP    236295-70000
DELI JARLSBERG DIP    237462-40000
JARLSBERG DIP    247199-00000
DELI JARLSBERG CHEESE DIP    286292-70000
DELI APPLEWOOD CHEDDAR DIP    286462-20000
DELI BUFFALO BLUE CHEESE SPREAD    295095-50000
DELI SOUTHWEST CHEESE SPREAD    295408-50000
DELI RANCH CHEESE SPREAD    295409-50000
Out of an abundance of caution, these items have been removed from store shelves and the company has initiated its customer recall notification system that alerts customers who may have purchased recalled products through register receipt tape messages and phone calls.
Customers who have purchased the product described above should not consume it and should return it to a store for a full refund or replacement. Additional questions can be directed to Kroger Customer Connect at (800) 576-4377.

Abdallah Candies Issues Allergy Alert on Undeclared Almond in Lund’s and Byerly’s 16 Oz. Sea Salt Caramels

August 12, 2020

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Abdallah Candies of Apple Valley, MN is voluntarily recalling a limited quantity of Lund’s and Byerly’s 16 oz. sea salt caramels with code AC31 on the bottom of the box. The boxes contain sea salt almond caramels instead of sea salt caramels.
Sea salt almond caramels contain almonds as an ingredient, which was not declared on the label. People who have an allergy or severe sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume these products.
Product was distributed in Minnesota and reached consumers only through Lund’s and Byerly’s grocery stores. The recalled products were distributed from 05/21/20 to 08/05/20. Retail products are packaged in candy boxes with a band around the box containing nutrition and ingredient information. The code AC31 is found on the outside packaging on the bottom side of the boxes. The company has not been notified of any illness associated with this product.
Consumers who purchased the product/code cited above are advised not to eat any product and should destroy or return the product to the place of purchase.
Consumers with questions should call Abdallah Candies with their concerns. Monday through Friday 8am to 4:30 pm central time at 952-890-4770 or 800-348-7328

Serafin Fishery Issues Allergy Alert on Undeclared Anchovies, Eggs, Milk and Soy in Salmon Dip and Whitefish Dip

August 13, 2020

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Serafin Fishery is recalling its 8-ounce containers of Salmon Dip and Whitefish Dip because they may contain undeclared anchovies, eggs, milk and soy. People who have allergies to anchovies, eggs, milk and soy run the risk of serious or life-threatening allergic reaction if they consume these products.
The recalled Salmon Dip and Whitefish Dips were distributed locally in Michigan retail stores.  The product comes in an 8-ounce, clear plastic package marked with lot #729 and lot #807 on the top and with expiration dates of August 12, 2020 and August 24, 2020 on the label.
No illnesses have been reported to date in connection with this problem.
The recall was initiated after it was discovered during an inspection conducted by the Michigan Department of Agriculture and Rural Development that the products’ labeling did not list all of the products’ ingredients. Production of the product has been suspended until FDA and the company are certain that the problem has been corrected.
Individuals with an allergy or sensitivity to anchovies, eggs, milk and soy should not consume these products. Households that include individuals with an allergy or sensitivity to any of these allergens should dispose of the recalled product.  Consumers who have purchased the 8-ounce packages of Salmon Dip and Whitefish Dip are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Serafin Fishery at 1-989-879-4596, Monday thru Friday from 9 to 5 p.m.

Kader Exports Recalls Frozen Cooked Shrimp Because of Possible Health Risk

August 12, 2020

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Kader Exports, with an abundance of caution, is recalling certain consignments of various sizes of frozen cooked, peeled and deveined shrimp sold in 1lb, 1.5lb., and 2lb. retail bags. The product has been distributed nationwide from late February 2020 to Mid-May 2020 because it has the potential to be contaminated with Salmonella.
Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
The affected product details are as below. The brand names of the products are: AQUA STAR RESERVE/ CENSEA/ FRESH MARKET/ KIRKLAND/ TOPS/ UNISTAR/ WELLSLEY FARMS.
Product Description    CODE
AQUA STAR RESERVE Cooked, Peeled and Deveined, Tail-on, 26/30 shrimp per pound, NET WT 1lbs    03467 0035 02, 03467 0036 02 & 03467 0037 02
AQUA STAR RESERVE Cooked, Peeled and Deveined, Tail-on, 31/40 shrimp per pound, NET WT 1lbs    03467 0035 02, 03467 0036 02 & 03467 0037 02
CENSEA Cooked, Tail Off, Shrimp, Peeled and Deveined, 31/40 shrimps per pound, NET WT 32Oz, 2lbs, 908g    26 0 007 D, 26 0 008 D & 26 0 009 D
CENSEA Cooked, Tail Off, Shrimp, Peeled and Deveined, 41/50 shrimps per pound, NET WT 32Oz, 2lbs, 908g    26 0 008 D
CENSEA Cooked, Tail Off, Shrimp, Peeled and Deveined, 61/70 shrimps per pound, NET WT 32Oz, 2lbs, 908g    26 0 009 D
FRESH MARKET Cocktail Shrimp, Fully Cooked, Tail on, Peeled and Deveined, 26/30 shrimp per pound, NET WT 24Oz, 1.5lbs, 680g    91H/29YD/AP-0007151/001, 91H/30YD/AP-0002092/001 & 91H/31YD/AP-0048718/001
KIRKLAND Signature Cooked, Peeled and Deveined, Tail-on, 31/40 shrimp per pound, NET WT 2lbs, 908g    02920 31122, 00230 31122 & 00330 31122
KIRKLAND Signature Cooked, Peeled and Deveined, Tail-on, Shrimps, 21/25 shrimp per pound, NET WT 2lbs, 908g    00820 31122, 00920 31122, 01020 31122 & 01120 31122
KIRKLAND Signature Cooked, Peeled and Deveined, Tail-off, 50/70 shrimps per pound, NET WT 2lbs, 908g    01410 31122, 01510 31122, 01610 31122 & 01710 31122
KIRKLAND Signature Cooked, Peeled and Deveined, Tail-on, Shrimps 31/40, NET WT 32 Oz, 2lbs, 908g    11829 31122, 11929 31122, 12029 31122, 12129 31122 & 00710 31122
UNISTAR White Shrimp Cooked 16/20 shrimp per pound, NET WT 32Oz, 2lbs, 908g    01-12-2020
UNISTAR White Shrimp Cooked 21/25 shrimp per pound, NET WT 32Oz, 2lbs, 908g    01-11-2020
UNISTAR White Shrimp Cooked 26/30 shrimp per pound, NET WT 32Oz, 2lbs, 908g    01-10-2020 & '01-11-2020
UNISTAR White Shrimp- Cooked, 26/30 shrimps per pound NET WT 32Oz, 2lbs, 908g    01-11-2020 & '01-12-2020
UNISTAR White Shrimp- Cooked, 20/40 shrimps per pound NET WT 32Oz, 2lbs, 908g    12-19-2019
UNISTAR White Shrimp-Cooked, 40/60 shrimps per pound NET WT 32Oz, 2lbs, 908g    12-20-2019
UNISTAR White Shrimp- Cooked, 60/80 shrimps per pound NET WT 32Oz, 2lbs, 908g    12-19-2019, 12-20-2019 & 12-21-2019
UNISTAR White Shrimp- Cooked, 80/120 shrimps per pound NET WT 32Oz, 2lbs, 908g    12-19-2019 & '12-21-2019
TOPS Cooked Shrimp, Peeled and Cleaned, Tail-on, COLOSSAL16/20 shrimp per pound, NET WT 16Oz,1lbs, 454g.    91H/24YD/AP-027193/001
TOPS Cooked Shrimp, Peeled and Cleaned, Tail-on, Extra Large 31/40 shrimp per pound, NET WT 16Oz,1lbs, 454g.    91H/26YD/AP-0011369/001
TOPS Cooked Shrimp, Peeled and Cleaned, Tail-on, Large 51/60 shrimp per pound, NET WT 16Oz,1lbs, 454g.    91H/24YD/AP-027193/001 & 91H/26YD/AP-0011369/001
WELLSLEY FARMS Extra Large Cooked Shrimp, Peeled and Deveined, Tail-on, 31/40 shrimps per pound, NET WT 32Oz, 2lbs, 907g    91H/18RN/AP-006327/001, 91H/19RN/AP-004552/002 & 91H/20RN/AP-0022178/002
WELLSLEY FARMS Extra Jumbo Cooked Shrimp, Peeled and Deveined, Tail-on, 21/25 shrimp per pound, NET WT 24Oz,1.5lbs, 680g    91H/26YD/AP-006327/001
WELLSLEY FARMS Extra Large Cooked Shrimp, Peeled and Deveined, Tail-on, 31/40 shrimps per pound, NET WT 32Oz, 2lbs, 907g    91H/27YD/AP-0000783/002
Products not bearing these codes are not affected or involved in this recall.
There have been no reports of any illnesses to date associated with these cooked shrimp distributions. However, cooked shrimp imported by Kader Exports was tested by the FDA and found to contain Salmonella. Kader Exports did not distribute and have agreed to voluntarily destroy cooked shrimp found violative. The probable root cause for this recall is cross contamination. The company has eliminated the source of contamination and preventive steps were taken.
Based on known consumption patterns it is believed most if not all the distributed products have been consumed, and any remaining product has been placed on hold subject to further evaluation.
Consumers who have purchased the above product are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at +91-022-62621004/ +91-022-62621009, Mon-Fri 10:00hrs -16:00hrs GMT+5.5.

Spokane Produce Inc. Issues Recall of Products Containing Onions Because of Possible Health Risk

August 11, 2020

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Spokane Produce, Inc. of Spokane, WA is voluntarily recalling salsa products containing onions as a result of the expanded onion recall initiated by Thomson International, Inc., which resulted in a recall by Spokane Produce’s onion supplier. These recalls are due to concerns of the potential for contamination by Salmonella spp.
Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
Product was distributed in ID, MT, OR, WA states and it reached consumers only through retail stores. The recalled products were distributed from 05/13/20 to 08/10/20. Retail products were packaged in 15oz. plastic tubs and institutional size one gallon plastic containers.
Spokane Produce’s products subject to the recall are listed in the table below.
ITEM NUMBER    PRODUCT NAME    SIZE    BEST BY DATE
83260    Saddlin' Up Salsa Hot    15 oz    8/16/2020
83259    Saddlin' Up Salsa Medium    15 oz    9/30/2020
83259    Saddlin' Up Salsa Medium    15 oz    8/5/2020
83258    Saddlin' Up Salsa Mild    15 oz    8/11/2020
84032    Salsa Verde    15 oz    8/26/2020
84044    Salsa Verde    Gallon    9/28/2020
84044    Salsa Verde    Gallon    8/11/2020
No other Spokane Produce’s products are impacted by this recall.
No illnesses have been reported in association with these salsa products to date.
Out of an abundance of caution, as a service to the general consuming public at large, product is being recalled in consultation with the Food and Drug Administration (FDA).
Consumers who purchased any of the products/best buy dates cited above are advised not to eat any product and should destroy or return the product to the place of purchase. Consumers with questions should call Spokane Produce, Inc., 10am-4pm (PST) at 509-710-8301.

Mr. Wok Foods, Inc. Recalls Multiple Meat and Poultry Products due to Misbranding and Undeclared Allergens

August 10, 2020

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WASHINGTON, Aug. 10, 2020 – Mr. Wok Foods, Inc., a Las Vegas, Nev. establishment, is recalling approximately 200,000 pounds of meat and poultry products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products may contain milk, wheat, soy, peanuts, or oysters, which are known allergens. The products may also contain MSG, sesame products, or sulfites, which are not declared on the product labels. 
The frozen meat and poultry items were produced from Aug. 6, 2019 through Aug. 6, 2020. This spreadsheet contains a list of the products subject to recall. [View Labels (PDF only)]
The products subject to recall bear establishment number “EST. 20783” or “P-20783” inside the USDA mark of inspection. These items were distributed for institutional use in vending machines and restaurants nationwide.                      
The problem was discovered by FSIS in-plant personnel during routine label reviews, when they found that one or more allergens were not listed on labels for various products.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers. When available, the retail distribution list will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Jae Hwang, General Manager, Mr. Wok Foods, Inc., at (626) 964-8230, ext. 122.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Soluciones Cosméticas Issues Voluntary Nationwide Recall of Bersih Hand Sanitizer Gel Due to The Potential Presence of Undeclared Methanol (Wood Alcohol)

August 9, 2020

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Soluciones Cosméticas voluntary recalled all lots of Bersih Hand Sanitizer Gel Fragrance Free sold in 16.9 ounce bottles to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol). This release provides additional information about the packaging for the recalled products.
Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date Soluciones Cosméticas has not received reports of adverse events related to this recall.
The product is used as a hand sanitizer and is packaged in 16.9 ounce plastic clear bottles with blue tops or green tops with UPC Codes 816822026667 or 7503007103178. The lot numbers range from 0100K01 to 0148K01. This product was distributed nationwide to wholesale distributors and retailers.
Soluciones Cosméticas is notifying its distributors by voluntary recall letter and consumers via this press release. Consumers that have the product subject to this recall should stop using and either contact Soluciones Cosméticas per the below for disposal instructions or return it to the place of purchase.
Consumers with questions regarding this recall can contact Soluciones Cosméticas at  866-912-8410 Monday through Friday 8am to 5pm Eastern Time or by email at bersihrecall6551@stericycle.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

FRESHOUSE II, LLC Voluntarily Recalls Select Mesh Bags and Bulk Shipments of Potatoes, Limes, Valencia Oranges and Lemons Because of Possible Health Risk

August 9, 2020

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Freshouse II, LLC of Salisbury, NC is recalling the following specific production lots, brands and weights of Valencia Oranges, Lemons, Limes, Organic Limes, and Red B Potatoes because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recall was voluntarily initiated after the company’s routine internal testing identified Listeria monocytogenes on a piece of equipment in one of our packing facilities. We have ceased the production and distribution of the product that was packed on the equipment in question and are taking corrective actions and continually evaluating our cleaning and sanitation regimes.
No illnesses have been associated with this recall to date.
Consumers can identify recalled retail products by looking for the brand, UPC number and, if available the trace number printed on the tag or clip attached to the opening end of the bag. The recalled products were shipped directly to retailer distribution centers in North Carolina, Pennsylvania, South Carolina, and Virginia and to wholesalers in Maryland and North Carolina (see table below). 
CONSUMER RETAIL ITEMS
Recall Initiated August 9, 2020
PRODUCT    BRAND    RETAIL UPC    TRACE # printed on tag or clip on bag    SIZE    LOT # ON BULK CASES
(this information is for retail stores)
Limes    Freshouse    33383 14683    174618 174570 174571 174572    2lb mesh bags    16444003
16444603
16444703
Organic Limes    Natures Promise    88267 53813    174375    1lb mesh bags    X0174375
Red B Potatoes    Fresh from the Start    33383 51003    174575
174403 174595    3lb mesh bags    16475401
16453501
16475401
Lemons    Fresh from the Start    33383 14020    174551 174552    2lb mesh bags    16453103
16415302
Lemons    Wegmans    77890 15917    n/a    2lb mesh bags    16453103
Valencia Oranges    Wegmans    77890 52363    n/a    4lb mesh bags    16415104
WHOLESALE BULK ITEMS
Recall initiated August 9, 2020
PRODUCT    SIZE    Shipper Reference Numbers
(this information is for
wholesale customers)
  Lemons    40 lb boxes    1187005, 1187128, 1187103, 1187112
  Limes    40 lb boxes    1187112, 1187099, 1187128, 1186832
  Red Potatoes    50 lb bags    1187098, 320873, 320992, 2182424
  Valencia Oranges    40 lb boxes    1187099, 1187015, 1187112
Consumers who have a recalled item listed above in their possession should not consume it and should destroy the product in a way so that it may not be consumed by others or return it to the place of purchase for a refund. Consumers with questions may contact Freshouse II, LLC at 631-369-7150, Monday through Friday: 8:00 am to 5:00 pm. Eastern Time. Consumers may also contact the company via email (customerservice@freshouse.com) or visit the company’s website at www.freshouserecall.comExternal Link Disclaimer.
Freshouse II, LLC has notified its retail and wholesale customers who received the recalled product directly from the company and is requesting that these customers remove the recalled product from commerce. We are also asking our direct customers to notify their customers of this recall. The company is issuing this press release and keeping the U.S. Food & Drug Administration informed of its recall process to assure that consumers are properly alerted.
“We voluntarily issued this recall out of an abundance of caution with the steadfast intent to minimize even the slightest risk to public health,” said Jamey Friedman, President. “We take food safety and this recall seriously. Freshouse is committed to providing consumers with fresh, nutritious, safe products.”

Wegmans Food Markets, Inc. Announces Recall of Select Valencia Oranges, Lemons, and Various Products Containing Fresh Lemon Because of Possible Health Risk

August 9, 2020

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Wegmans Food Markets, Inc. is recalling its four-pound bag of Valencia Oranges, two-pound bag of lemons, bulk lemons, and a variety of in-store produced seafood and restaurant foods items that contain fresh lemon because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeriaem> infection can cause miscarriages and stillbirths among pregnant women.
The affected products were sold in Wegmans stores in New Jersey, Pennsylvania, Virginia, North Carolina, Maryland, and Brooklyn and Harrison, NY.
Affected produce items, sold between July 31 and August 7, 2020, include:
Wegmans 4lb Bag Valencia Oranges – UPC: 7789052363
Wegmans 2lb Bag Lemons – UPC: 7789015917
Wegmans bulk lemons – UPC: 4033
The lemons and oranges were supplied to Wegmans by Freshouse Produce LLC of Salisbury, NC, which issued a voluntary recall after the company’s internal testing identified Listeria monocytogenes on a piece of equipment in one of its packing facilities. No illnesses associated with this recall have been reported to Wegmans or its supplier.
Wegmans has placed automated phone calls to alert customers who purchased these products using Shoppers Club.
Customers should return these products to the service desk for a full refund. Those with questions may contact Wegmans Food Markets 1-855-934-3663 Monday through Friday from 8:00 a.m. - 7:00 p.m. or Saturday and Sunday from 8:00 a.m. - 5:00 p.m.

Progressive Produce Voluntarily Recalls Red and Yellow Onions Because of Possible Health Risk

August 10, 2020

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Progressive Produce LLC is voluntarily recalling a very limited quantity of red and yellow onions as a result of a recall initiated by Thomson International, Inc., which supplied affected onions to Progressive Produce. This recall is being made out of an abundance of caution due to the potential for contamination with Salmonella.
The recalled products were sold on the West Coast, at Trader Joe’s (conventional red onions sold only in Arizona, California, Nevada, and Utah stores) and Ralph’s (conventional yellow onions sold only in California stores). The onions are sold loose in bulk bins. The red onions have a PLU sticker with the brand name Pacific Gold. No other Progressive Produce onions or other products are impacted by this recall.
Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
Retailers that received recalled product from Progressive Produce have been instructed to remove any recalled product from their shelves and to dispose of any product that is remaining in their inventory.
Consumers who have purchased recalled products are urged not to consume them and to dispose of them immediately or to return them to the store for a full refund. Consumers may email Progressive Produce for further information at foodsafety@progressiveproduce.com. Consumers with concerns about an illness from consumption of the recalled products should contact a health care provider.
Progressive Produce has not received any reports of illnesses to date associated with these recalled items, although a current illness outbreak appears to be associated with certain onions supplied to a number of companies by Thomson International.
Progressive Produce is cooperating fully with FDA to facilitate the efficient recall of these onions. A photo of the red onion label is attached.

Taylor Farms Issues Recall of Products Containing Onions Because of Possible Health Risk

August 6, 2020

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Taylor Farms Texas, a Dallas, TX establishment, is voluntarily recalling products containing onions as a result of the expanded onion recall initiated by Thomson International, Inc., which resulted in a recall by Taylor Farms’ onion supplier. These recalls are due to concerns of the potential for contamination by Salmonella spp.
Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
The Taylor Farms TX products subject to the recall are limited to the code dates listed below. No other Taylor Farms products are impacted by this recall.
Store Name    Product Description    UPC    Best If Used By Date    Lot Codes    Products Shipped to Select Stores in These States
Kroger    Taylor Farms Macaroni Salad, 9.9 oz. container    030223015642    8/5/2020
8/6/2020    TFD212
TFD213    LA, TX
Kroger    Taylor Farms Rotini Pasta Salad, 10 oz. container    030223002789    8/5/2020
8/6/2020    TFD212
TFD213    LA, TX
Kroger    Taylor Farms Chicken Salad Croissant Sandwich, 6.25 oz.    03223028611    8/3/2020
8/4/2020    TFD212
TFD213    LA, TX
Walmart    Marketside Diced Yellow Onion 3/8", 8 oz. tray    681131328739    8/11/2020    TFD212    CO, IA, IL, KS, MO, ND, NE, OK, SD
Walmart    Marketside Diced Mirepoix, 10 oz. tray    681131276511    8/10/2020    TFD212    CO, IA, IL, KS, MO, ND, NE, OK, SD
Walmart    Marketside Fajita Stir Fry, 8 oz. tray    681131093026    8/10/2020    TFD212    CO, IA, IL, KS, MO, ND, NE, OK, SD
Walmart    Taylor Farms Chicken Salad Croissant Sandwich, 6.25 oz.    030223110095    8/4/2020
8/5/2020    TFD212
TFD213    TX
Taylor Farms has not received any reports of illnesses to date associated with these recalled items. The recalled products were distributed from 07/30/2020 – 08/01/2020. The retailers involved have been instructed to remove any remaining product from their shelves and to dispose of any of the remaining product in their inventory.
Customers who have purchased these products are urged not to consume the products and should dispose of the recalled products immediately. Consumers may call for further information at (855) 455-0098 between the hours of 9 am (CST) and 5 pm (CST) Monday through Friday. Consumers with concerns about an illness from consumption of this product should contact a health care provider.

Haven’s Kitchen Home, LLC Issues Allergy Alert on Undeclared Soy in Product

August 7, 2020

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Haven’s Kitchen, legally known as Haven’s Kitchen Home, LLC of New York, NY is voluntarily recalling one lot of Golden Turmeric Tahini sauce because it may contain Gingery Miso sauce which contains undeclared soy. People who have an allergy or severe sensitivity to soy run the risk of serious or life- threatening allergic reaction if they consume this mislabeled product.
Product was distributed to the following United Natural Foods Inc. (UNFI) and Dora’s Naturals locations:
UNFI    Atlanta, Georgia
UNFI    Chesterfield, New Hampshire
UNFI    Greenwood, Indiana
UNFI    Hudson Valley, New York
UNFI    Lancaster, Texas
UNFI    Moreno Valley, California
UNFI    Racine in Sturtevant, Wisconsin
UNFI    Richburg, South Carolina
UNFI    Ridgefield, Washington
UNFI    Rocklin, California
UNFI    Sarasota, Florida
Dora’s Naturals in South Hackensack, NJ
The product comes in 5oz pouches under the name Haven’s Kitchen Golden Turmeric Tahini with the Unit UPC Code: 8-18758-02011-5. The product in question has an expiration date of 10/23/20 and a lot code of 1770.
This recall only affects this singular lot code/date code of Golden Turmeric Tahini. No other sauces are affected by this recall. No illnesses have been reported to date.
The recall was initiated after it was discovered that pouches labeled Golden Turmeric Tahini were filled with another flavor of our sauce that contains soy. Our manufacturer is investigating how the error occurred and is making any necessary changes to their production and packaging processes to ensure accuracy for our products.
Consumers are asked to check their refrigerators and dispose of the product affected by this recall. If you have any questions or need a replacement coupon for any product included in this recall, contact our Consumer Relations team at info@havenskitchen.com or (401) 315-4337 Monday – Friday from 9am est. – 5pm est.
Any consumers concerned about an illness should contact a physician. Anyone diagnosed by a physician as having an illness related to soy allergen is also urged to contact state and local public health authorities.

Giant Eagle Voluntarily Issued August 1st Recall of Onions and Prepared Foods Using Onions as an Ingredient Due to Potential Salmonella Contamination

August 6, 2020

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After receiving notification from onion supplier, Onion 52, that the vendor had sourced onions affected by the recent salmonella-related Thomson International, Inc. onion recall for Giant Eagle, the company pulled all impacted product on Saturday, August 1.
Giant Eagle recalled red, yellow and white onions sold in produce departments across Pennsylvania, Ohio, West Virginia, Indiana and Maryland. The recall also includes select prepared foods items that included the affected onions as ingredients sold across the same five states. The recall announcement is regarding potential salmonella contamination of the onions.
Out of an abundance of caution, Giant Eagle promptly removed these products on Saturday, August 1, from its produce and prepared foods departments as soon as it became apparent that some of its onion product may have been affected by the ongoing salmonella outbreak investigation by the FDA and CDC. Three are no reported illnesses among Giant Eagle customers to date associated with this recall.
Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems, can cause salmonellosis. Salmonellosis is one of the most common bacterial foodborne illnesses, and some symptoms of salmonellosis are diarrhea, abdominal cramps and a fever anywhere between 12 to 72 hours after consumption. This illness can last between four to seven days.
Recalled Onions Sold in Giant Eagle Produce Departments
Giant Eagle has recalled all bulk and bagged red, yellow and white onions sold in its produce department since June 6, 2020.
Customers who have purchased the affected product and are still in possession of it should dispose of it. Customers may also bring in the qualifying receipt to their local Giant Eagle or Market District location to receive a refund on their purchase of the impacted product.
For questions, customers may contact Onions52 at (801) 773-0630 or by email at customerservice@onions52.com.
Recalled Prepared Foods Items with Onion as Ingredient
Giant Eagle’s onion recall also included select prepared foods items purchase since July 25, 2020 that include onion as an ingredient. Impacted items include:
TUSCAN CHICKEN SALAD    20500200000
MD CAPRESE SALAD    20660900000
CHICKPEA & CARROT SALAD GREEK DRESSING    20686300000
SPINACH SALAD WITH RANCH DRESSING    20730400000
GREEN BEAN PORTABELLA    21660900000
HALF ITALIAN SUB    21665100000
FARMERS SALAD    21738800000
CUCUMBER TOMATO SALAD    22657400000
MD BLT SALAD    22657700000
MD BUFFALO CHICKEN SALAD    22658400000
COUNTRY STYLE PASTA SALAD FRENCH DRESSING    22658500000
GREEK SALAD LARGE    22660900000
GRILLED VEGETABLES    22664600000
MD GREEK SALAD WITH GREEK DRESSING    22665100000
MD G&G GREEK SALAD    22667100000
GE EGG & BACON SALAD WITH FRENCH DRESSING    23657100000
MD PHILLY STYLE STEAK STROMBOLI COLD    23660700000
CAJUN STYLE CHICKEN MEAL    23662500000
MD DIP-REUBEN    23665100000
MD GREEK SALAD WITH BALSAMIC DRESSING    23676600000
STUFFING BALLS S0678/1602    24658700000
22INCH ITALIAN HOAGIE    24659500000
SPECIALTY 12" ITALIAN HOAGIE    24660600000
CHEESEBURGER PIZZA SLICE    25048600000
PHILLY STEAK PIZZA SLICE    25049300000
PIEROGIE LASAGNA ROLL UP    25049400000
HOMEMADE MACARONI SALAD    25060700000
SPANIKOPITA    25061200000
12" DELUXE PIZZA    25065000000
DELUXE ITALIAN PARTY HOAGIE    25067800000
VEGETABLE PIZZA SLICE    25070900000
12" VEGETABLE PIZZA    25071800000
SHEET VEGETABLE PIZZA    25085100000
STUFFED BONE IN CHICKEN BREAST GOURMET    25086400000
STUFFED BONELESS CHICKEN BREAST GOURMET    25086700000
STUFFED TURKEY BREAST GOURMET    25086800000
POTATO AND CHEESE PIEROGIES    25089000000
COLD ITALIAN HERO, 12"    25089400000
ITALIAN HERO, 6", COLD    25093400000
SPINACH DIP DELI SERVICE CASE    25118000000
SPINACH DIP GRAB & GO    25118500000
MD EGG & BACON SALAD WITH LITE BALSAMIC DRESS    25118600000
CUCUMBER SALAD    25139500000
SANDWICH TOPPERS PLATTER -UP TO 25 SANDWICHES    25139600000
ZUCHINNI PANCAKES    27665100000
SAUSAGE PEPPERS AND ONIONS OVER PENNE    27697700000
MD S&F: SMOKE-STACKED SANDWICH    27751700000
CALIFORNIA COBB - SMALL    28659400000
Customers who have purchased the affected product and are still in possession of it should dispose of it. Customers may also bring in the qualifying receipt to their local Giant Eagle or Market District location to receive a refund on their purchase of the impacted product. For a complete list of items, please visit https://www.gianteagle.com/product-recallExternal Link Disclaimer.
Consumers with questions may contact Giant Eagle at 1-800-553-2324 Monday through Friday 9AM – 9PM.
In addition to this public communication regarding this recall, Giant Eagle initiated its consumer recall telephone notification process. The consumer recall process uses purchase data and consumer telephone numbers housed in the Giant Eagle Advantage Card database to alert those households that purchased the affected product and have updated telephone contact information in the database.
Contact: Dan Donovan
Giant Eagle, Inc.
412.967.4551
media.relations@gianteagle.com

FSIS Issues Public Health Alert For Ready-to-Eat Meat and Poultry Products Containing FDA-Regulated Onions that have been Recalled due to Possible Salmonella Newport Contamination

August 6, 2020

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WASHINGTON, Aug. 5, 2020 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) meat and poultry products containing Food and Drug Administration (FDA) regulated onions that have been recalled by Thomson International Inc. due to concerns that the products may be contaminated with Salmonella Newport. FSIS is issuing this public health alert out of the utmost of caution to ensure that consumers are aware that these products, which bear the USDA mark of inspection, should not be consumed. As more information becomes available, FSIS will update this public health alert.
The RTE meat and poultry items were produced by Taylor Farms on July 30 and 31, 2020. The following products are subject to the public health alert: [View Label (PDF only)] 
•    7.25-oz. plastic sealed container labeled as “Sausage Breakfast Scramble Bowl” with lot code TFD212AU8 and TFD213AU8 and with a best if used by 08/06/2020 or 08/07/2020.
•    6.2-oz. plastic sealed container labeled as “Taylor Farms Cheddar Cheese & Chicken Salad Snack Tray” with use by date 08/06/20 or 08/07/20 and lot code TFD212AU7 and TFD213AU7.
•    41.35-oz. plastic bags containing “Chicken Salad” with use by date 08/04/20 or 08/05/20 and lot codes TFD212AU8 and TFD213AU8.
•    10-oz. plastic sealed container labeled as “Chicken Salad Deli Snack” with lot codes TFD212AU3 and TFD213AU3 with best by dates 08/06/2020 or 08/07/2020.
•    7.75-oz. plastic sealed container labeled as “H.E.B. Shake Rattle Bowl SOUTHWEST SALAD with CHICKEN” and a best if used by date of “Aug 10/2020 and lot code TFD213AU20.
•    17.25-oz. plastic sealed container labeled as “Marketside SOUTHWEST STYLE SALAD WITH CHICKEN” with a best if used by date of 08/11/20 or 08/12/2020 and lot codes TFD212AU26 or TFD213AU26.
The products bear the establishment number “"P-34733" or "34733" inside the USDA mark of inspection or printed on the container. These products were shipped to retail locations in Arkansas, Louisiana, Mississippi, Oklahoma and Texas. 
CDC, FDA and public health and regulatory officials in several states are investigating a multistate outbreak of Salmonella infections linked to onions produced by Thomson International, Inc. There have been no confirmed reports of illness due to consumption of the FSIS-regulated products produced containing these onions. Anyone concerned about an illness should contact a health care provider.
FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
Salmonella can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. 
Consumers with questions can contact Kim Earnshaw or Elizabeth Llanes with Thomson International, Inc., at (661) 845-1111.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

SmithFoods Inc. Issues Allergy Alert on Undeclared Cashew Allergen in Earth Grown Vegan Non Dairy Almond Based Frozen Desserts

July 31, 2020

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SmithFoods Inc. announced that it is voluntarily recalling 16-oz pint packages of Earth Grown Vegan Non-Dairy Almond Based Frozen Desserts because it may contain an undeclared cashew allergen. People who have an allergy or severe sensitivity to cashews run the risk of a serious or life-threatening allergic reaction if they consume these products.
The recalled product was available for purchase at ALDI stores in Alabama, Arkansas, California, Connecticut, Delaware, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, Vermont, Wisconsin and West Virginia. The product was also available for purchase by ALDI customers through the company’s partnership with Instacart, a grocery delivery service.
Recalled UPC and lot codes are:
Description    Size    UPC    Lot/Best By Code
Earth Grown Mocha Fudge Non-Dairy Frozen Dessert    16-oz /Pint    4099100002836    07-29-2021, 07-30-2021
Earth Grown Chocolate Non-Dairy Frozen Dessert    16-oz/Pint    4099100002850    07-26-2021, 07-27-2021
Earth Grown Vanilla Non-Dairy Frozen Dessert    16-oz/Pint    4099100002843    07-27-2021, 07-28-2021, 07-29-2021
The recall was initiated following a consumer complaint. The company continues to go through root cause analysis and is conducting a detailed review of allergen controls within all aspects of operations and supply chain processes.
There has been one reported incident of an allergic reaction to date.
The company has notified ALDI and ALDI stores will be removing the product from the shelves.
Consumers who have pints of Earth Grown Non-Dairy Almond Based Frozen Dessert with the codes listed should stop using and return them to the place of purchase for a refund. Consumers may contact Customer Contact at 800-776-7076 Monday through Friday from 8a-5p ET.

SmithFoods Inc. Issues Allergy Alert on Undeclared Cashew Allergen in Earth Grown Vegan Non Dairy Almond Based Frozen Desserts

July 31, 2020

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SmithFoods Inc. announced that it is voluntarily recalling 16-oz pint packages of Earth Grown Vegan Non-Dairy Almond Based Frozen Desserts because it may contain an undeclared cashew allergen. People who have an allergy or severe sensitivity to cashews run the risk of a serious or life-threatening allergic reaction if they consume these products.
The recalled product was available for purchase at ALDI stores in Alabama, Arkansas, California, Connecticut, Delaware, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, Vermont, Wisconsin and West Virginia. The product was also available for purchase by ALDI customers through the company’s partnership with Instacart, a grocery delivery service.
Recalled UPC and lot codes are:
Description    Size    UPC    Lot/Best By Code
Earth Grown Mocha Fudge Non-Dairy Frozen Dessert    16-oz /Pint    4099100002836    07-29-2021, 07-30-2021
Earth Grown Chocolate Non-Dairy Frozen Dessert    16-oz/Pint    4099100002850    07-26-2021, 07-27-2021
Earth Grown Vanilla Non-Dairy Frozen Dessert    16-oz/Pint    4099100002843    07-27-2021, 07-28-2021, 07-29-2021
The recall was initiated following a consumer complaint. The company continues to go through root cause analysis and is conducting a detailed review of allergen controls within all aspects of operations and supply chain processes.
There has been one reported incident of an allergic reaction to date.
The company has notified ALDI and ALDI stores will be removing the product from the shelves.
Consumers who have pints of Earth Grown Non-Dairy Almond Based Frozen Dessert with the codes listed should stop using and return them to the place of purchase for a refund. Consumers may contact Customer Contact at 800-776-7076 Monday through Friday from 8a-5p ET.

H-E-B Issues Recall for Blue Cheese Salmon Burgers Due to Undeclared Wheat

August 4, 2020

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Products contain wheat, a known allergen, which is not declared on the product label
H-E-B is voluntarily issuing an all-store recall for Blue Cheese Salmon Burgers due to an undeclared allergen. The products contain wheat, a known allergen, which is not declared on the product label. People who have an allergy or severe sensitivity to wheat run the risk of serious or life-threatening allergic reaction if they consume these products.
All affected product has been removed from store shelves. There has been one reported illness to date.
Blue Cheese Salmon Burgers affected by this recall were sold behind the seafood counter, in the seafood department and in the meal simple area in H-E-B retail stores throughout Texas. This voluntary recall impacts the following products with dates with dates up to and including 8/3/2020:
UPC    Item description
23757500000    Meal Simple SC SAL BURGER BLUE CHS 2CT
23759000000    Meal Simple SC SAL BURGER WILD BLUE CHS
23725500000    SALMON/BURGER BLUE CHEESE TP
22528700000    SALMON/BURGER BLUE CHEESE
23731100000    SALMON/BURGER WILD BLUE CHS TP
23711100000    SALMON/BURGER WILD BLUE CHEESE
Affected products can be returned to the store for a full refund. Customers with any questions or concerns can contact H-E-B Customer Relations at 1-855-432-4438 Monday through Friday from 8 a.m. to 5 p.m. Central Standard Time.
Company Contact Information
Consumers:
H-E-B Customer Relations
 1-855-432-4438 

LABORATORIOS JALOMA S.A. de C.V. Issues Voluntary Recall of the Jaloma Antiseptic Hand Sanitizer Due to the Potential Presence of Undeclared Methanol

August 1, 2020

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LABORATORIOS JALOMA S.A. de C.V. is voluntarily recalling all lots and all bottle sizes of the Jaloma Antiseptic Hand Sanitizer, Ethyl Alcohol 62% With vitamin E to the consumer level. This recall has been initiated because FDA sampled the 500 mL product and found it to be contaminated with undeclared methanol (wood alcohol). Although the contamination was linked to the 500 mL product, due to the abundance of caution, Jaloma is recalling all lots of all sizes within expiry. The NDCs, lot #s, and expiration dates are listed in the table below.
Risk Statement: Substantial methanol exposure could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, and permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, LABORATORIOS JALOMA S.A. de C.V. has not received any reports of adverse events related to this recall.
Recalled Products
Product(s)    NDCs    Sizes    UPC    Lot #s & Expiration Dates
Jaloma Antiseptic Hand Sanitizer
Ethyl Alcohol 62%
With vitamin E    65055-600-02    16.9 fl oz.
(1.06 pt) (500 mL)    7 59684 51503 3    0005295
Exp: April, 2022
0006373
Exp: May, 2022
Jaloma Antiseptic Hand Sanitizer
Ethyl Alcohol 62%
With vitamin E    65055-600-01    4 fl oz
(120 mL)    7 59684 51502 6    0005412
Exp: April, 2022
0007134
Exp: May, 2022
0007834
Exp: May, 2022
0009239
Exp: June, 2022
The product is used as a hand sanitizer for hand washing to decrease bacteria on the skin when soap and water are not available. The products are distributed in a 4 fl oz (120 mL) Polyethylene Terephthalate (PET) plastic bottle and a 16.9 fl oz (1.06 pt) (500 mL) PET or High-density polyethylene (HDPE) plastic bottle.  Product is labeled with a red logo with the word Jaloma written in white letters. The product was distributed throughout the United States.  It was imported to one (1) wholesaler and two (2) distributors.
Each product contains a lot number and expiration date stamped directly on the bottle or on the label of the 16.9 fl oz HDPE bottle in the format below.  See table for lot numbers of each individual bottle.
0007834
EXP0522
LABORATORIOS JALOMA S.A. de C.V. is notifying its customers/distributors by recall letter and consumers via this press release. LABORATORIOS JALOMA S.A. de C.V.is arranging for return and refund of all recalled products.
Consumers/distributors/retailers that have the product subject to this recall should stop using/distributing the Jaloma Antiseptic Hand Sanitizer and return it to the place of purchase.
Consumers with questions regarding this recall can contact LABORATORIOS JALOMA S.A. de C.V. during business hours: 9:00am – 5:00pm (CT)
Toll Free: + 52 1 800 120 0202
Email: asuntosregulatorios@jaloma.com.mx
Consumers should contact their physician or healthcare provider if they experienced any problems that may be related to taking or using this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Albek de Mexico S.A. de C.V. Issues Voluntary Nationwide Recall of All Hand Sanitizers Within Expiry Due to Potential Presence of Methanol (Wood Alcohol)

July 31, 2020

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Albek de Mexico S.A. de C.V is voluntarily recalling all lots and all brands of hand sanitizer currently in US distribution to the consumer level. This recall is being initiated out of an abundance of caution due to detection of methanol in hand sanitizer samples manufactured by Albek when product was presented for import into the United States.
Risk Statement: Substantial methanol exposure could result in serious health effects (including nausea, diarrhea, vomiting, severe abdominal pain, headache, blurred vision, permanent blindness, seizures, coma, nervous system damage) or death. Persons using methanol-based products on their hands may be at risk. Young children who accidently ingest them and adolescents and adults who drink such products are most at risk for methanol poisoning. To date, there have been no reports of serious adverse events related to the products in the scope of this recall.
The products are labeled for use as a hand sanitizer (or “antiseptic”) and are packaged for several nationwide distributors in a variety of formats as indicated in the table as follows:
Item    Nuuxsan    Modesa    Assured    Assured    Next Product Name 

Nuuxsan Instant Hand Sanitizer    Modesa Hand Sanitizer with Moisturizers and Aloe Vera    Assured Hand Sanitizer Vitamin E and Aloe    Assured Hand Sanitizer Aloe Vera    Next Hand Sanitizer
NDC    72758-005-02, 72758-001-08    72758-011-23    72758-010-23    72758-009-23    50066-605-08
Package Format(s)    8 fl oz plastic bottles    8 fl oz plastic bottles    8 oz. plastic bottles<    8 oz. plastic bottles    8 oz. plastic bottles
UPC    713620000175    32251380426    639277928597    639277928610    650240053573
Afected Lot Number(s)    All Lots    1931104AL    1931101AL    1931102AL    The affected lots are those that end 1001,
1002, 1003, 1004, 1005.
Product Name    NDC    UPC and Lot    Volume/Package
Assured Hand Sanitizer with Vitamin E and Aloe    72758-010-23    639277928597    8 oz. plastic bottles
Modesa Hand Sanitizer with Moisturizers and Aloe Vera    72758-011-23    639277928610    8oz. plastic bottles
Modesa Hand Sanitizer with Moisturizers and Vitamin E    72758-012-23    Never Produced
Next Hand Sanitizer    50066-605-08    650240053573    8oz. plastic bottles
Assured Hand Sanitizer Aloe Vera    72758-009-23    639277928610    8 oz. plastic bottles
Nuuxsan Instant Hand Sanitizer    72758-005-02    713620000175    8oz. plastic bottles
NuuxSan Instant Hand Sanitizer    72758-001-08    713620000175    8oz. plastic bottles
This NDC was created in 2019 and then replaced by NDC 72758-002-08.
The products were distributed nationwide in the United States beginning on November, 15 2019.
Albek is partnering with its distributors, who will help notify their customers by phone calls, emails, and/or mailed letters and is arranging for return of all recalled products. Consumers, distributors, and retailers that have product which is being recalled should stop use or distribution and return to place of purchase.
Consumers with questions regarding this recall can contact Mrs. Susana Luna (713)961-0262, [days of week] from [state time and zone] or e-mail to contact@albek.com.mx. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using these products.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Thomson International Inc. Conducts Voluntary Recall of Red, Yellow, White, and Sweet Yellow Onions Because of Possible Salmonella Risk

August 3, 2020

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Thomson International Inc. of Bakersfield, California is recalling Red, Yellow, White, and Sweet Yellow Onions shipped from May 1, 2020 through the present.  The onions are being recalled because they have the potential to be contaminated with Salmonella, an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
Onionswere distributed to wholesalers, restaurants, and retail stores in all 50 states, the District of Columbia and Canada.
The onions were distributed in 5 lbs. carton. 10 lbs. carton. 25 lbs. carton. 40 lbs. carton, 50 lbs. carton. bulk, 2 lb. mesh sacks, and 3 lb. mesh sacks, 5 lb. mesh sacks, 10 lb. mesh sacks 25 lbs. mesh sacks, 50 lbs. mesh sacks under the brand names Thomson  Premium, TLC Thomson International, Tender Loving Care, El Competitor, Hartley’s Best, Onions 52, Majestic, Imperial Fresh, Kroger, Utah Onions and Food Lion.
Consumers, restaurants, and retailers should not eat, sell, or serve red, white, yellow, or sweet onions from Thomson International, Inc. or products containing such onions. If you cannot tell if your onion is from Thomson International Inc., or your food product contains such onions, you should not eat, sell, or serve it, and should throw it out.
The U.S. Food and Drug Administration, along with the U.S. Centers for Disease Control and Prevention, is investigating a multistate outbreak of Salmonella Newport infections that may be linked to these onions, so Thomson International is recalling the onions out of an abundance of caution.  As of now no specific source of contamination or contaminated shipment has been identified, and FDA is also investigating other potential sources of contamination and has not yet reached a final conclusion.
396 total illnesses have been reported to date including 59 hospitalizations.  States with cases include: AK (6), AZ (14), CA (49), CO (10), FL (3), ID (5), IL (10), IN (2), IA (15), KS (1), KY (1), ME (4), MD (1), MI (23), MN (10), MO (6), MT (33), NE (5), NV (5), NY (4), NC (3), ND (5), OH (7), OR (71), PA (2), SC (1), SD (11), TN (5), TX (1), UT (61), VA (4), WA (2), WI (5), and WY (11).
Consumers who have any Red, Yellow, White, and Sweet Yellow Onions under the above brand names, or who cannot tell if their onions are from Thomson International, should immediately discard these products and disinfect any surfaces that came into contact with the onions.   Consumers with questions may contact the company by calling Kim Earnshaw at 661-845-1111

JBS Food Canada ULC Recalls Raw Boneless Beef Products Distributed without Benefit of Import Re-inspection

July 31, 2020

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WASHINGTON, July 30, 2020 – JBS Food Canada ULC, a Brooks, Alberta, Canada establishment, is recalling approximately 38,406 pounds of boneless beef head meat products that were not presented for import re-inspection into the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The raw, frozen, boneless beef head meat items were imported on July 13, 2020 and were further processed by another company into ground beef products. The following products are subject to recall: [View Labels (PDF only)]
•    80-lb. boxes containing eight, 10-lb. chubs of “BALTER MEAT COMPANY 73/27 GROUND BEEF,” with “USE BY/FREEZE BY” dates of 08/09/2020 or 08/10/2020, pack dates of 072020, 072120, or 072220, and lot codes of 2020A or 2030A represented on the label.
The products subject to recall bear establishment number “EST. 11126” inside the USDA mark of inspection. These items were shipped to distribution centers in Florida, Georgia, North Carolina, and South Carolina, for further distribution to retail locations.
The problem was discovered when FSIS determined through routine surveillance that the product had by-passed FSIS import reinspection.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at https://www.fsis.usda.gov/recalls.
Consumers with questions about the recall can contact the JBS USA Consumer Hotline at (800) 727-2333. Members of the media with questions about the recall can contact Cameron Bruett, Sustainability & Corporate Communications, JBS USA, at (970) 506-7801 or cameron.bruett@jbssa.com.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

4e Brands North America Issues Expanded Nationwide Voluntary Recall of Hand Sanitizer Due to Potential Presence of Undeclared Methanol (Wood Alcohol)

July 30, 2020

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WASHINGTON, July 30, 2020 – JBS Food Canada ULC, a Brooks, Alberta, Canada establishment, is recalling approximately 38,406 pounds of boneless beef head meat products that were not presented for import re-inspection into the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The raw, frozen, boneless beef head meat items were imported on July 13, 2020 and were further processed by another company into ground beef products. The following products are subject to recall: [View Labels (PDF only)]
•    80-lb. boxes containing eight, 10-lb. chubs of “BALTER MEAT COMPANY 73/27 GROUND BEEF,” with “USE BY/FREEZE BY” dates of 08/09/2020 or 08/10/2020, pack dates of 072020, 072120, or 072220, and lot codes of 2020A or 2030A represented on the label.
The products subject to recall bear establishment number “EST. 11126” inside the USDA mark of inspection. These items were shipped to distribution centers in Florida, Georgia, North Carolina, and South Carolina, for further distribution to retail locations.
The problem was discovered when FSIS determined through routine surveillance that the product had by-passed FSIS import reinspection.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at https://www.fsis.usda.gov/recalls.
Consumers with questions about the recall can contact the JBS USA Consumer Hotline at (800) 727-2333. Members of the media with questions about the recall can contact Cameron Bruett, Sustainability & Corporate Communications, JBS USA, at (970) 506-7801 or cameron.bruett@jbssa.com.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Resource Recovery & Trading, LLC.,Issues Nationwide Recall of Hand Sanitizer Due to Potential Presence of Methanol (Wood Alcohol) and Subpotency Ethyl Alcohol Company Announcement

July 30, 2020

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RESOURCE RECOVERY & TRADING LLC, is voluntarily recalling all the lots manufactured by MXL Comercial S.A. de C.V. of Hand Sanitizer with the next information: HAND SANITIZER 70% Ethyl Alcohol Disinfectant Gel, packaged in 6.7 FL Oz. (200 ml) bottles, UPC 650240026020 and HAND SANITIZER Non-sterile Solution 70% Topical Solution, packaged in 20L (5.28 Gal) liter plastic containers, UPC 37710600013 to the consumer level. The products are being recalled due to the potential presence of undeclared methanol (wood alcohol) and subpotency ethyl alcohol.
Risk Statement: The main concern with the use of hand sanitizer that is sub-potent for ethyl alcohol is the potential for decreased bactericidal and virucidal activity. Adverse health consequences can be related to increased infections. In addition substantial, undeclared methanol exposure, which has inferior antiseptic properties compared to ethanol, can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, RESOURCE RECOVERY & TRADING LLC has not received any reports of adverse events related to this recall.
The product is used as a hand sanitizer to decrease germs when soap and water is not available and is packaged in 200 ml plastic bottles and 20 liter plastic containers. The product can be identified by the label below.
The product was distribution between June 10, 2020 and June 20, 2020 in the states of Alabama and Georgia.
RESOURCE RECOVERY & TRADING LLC is notifying its distributors and customers by phone calls and emails and is arranging for return and destruction of all recalled products.
Consumers/distributors/retailers that have product which is being recalled should stop using products, initiate recalls to the user level, and return all products to the place of purchase.
Consumers with questions regarding this recall can contact RESOURCE RECOVERY & TRADING LLC by phone (858) 964-4590 or e-mail to admin@rr-t.net. Monday to Friday from 9:00 am and 3:00 pm Pacific Time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Wellements LLC Issues Allergy Alert On Undeclared Milk Allergen In Two Lots Of Iron Drops And Iron Drops Sample

July 30, 2020

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Wellements LLC of Scottsdale, Arizona, is issuing a voluntary recall of two lots of its 1oz/30ml bottle of Iron Drops (UPC 729609000098) liquid Dietary Supplement and the sample version being Iron Drops Sample liquid Dietary Supplement because they may contain an undeclared milk allergen. People who have an allergy or severe sensitivity to milk allergens run the risk of serious allergic reaction if they consume these products. The recalled Iron Drops were distributed from 5.1.2019 to 7.22.2020 nationwide through select retail stores, Amazon.com and Wellements.com. The recalled Iron Drops Sample was distributed from 5.1.2019 to 7.22.2020 nationwide through promotional giveaways in select consumer purchases and select partners. Wellements Iron Drops are indicated for use in Infants 4 months to Children 3 years of age.
Wellements Iron Drops are sold in a 1oz glass amber bottle and packaged in an individual product carton that includes a 1ml oral syringe dispenser. The Wellements Iron Drops Sample is contained in a 1oz glass amber bottle filled to 2ml and packaged in an individual “SAMPLE- NOT FOR RESALE” product carton that includes a 1ml oral syringe dispenser.
The recalled products lot coding is located on the bottom of the bottle in yellow ink and on the side, towards the bottom of the carton in black ink. The recalled product coding is as follows:

Iron Drops Lot 18491 BB 1/2021

Iron Drops Lot 10592 BB 10/2020

Iron Drops Sample Lot 10592 BB 10/2020

There has been one allergic reaction reported to Wellements to date.
The recall was initiated after it was discovered that product containing a milk allergen was distributed in packaging that did not reveal the presence of a milk allergen. Wellements LLC was informed that one of the raw material ingredients used in Wellements Iron Drops and Iron Drops Sample was mistakenly blended with lactose, a milk constituent that contained milk allergen, by its manufacturer before being supplied for the production of Wellements finished Iron Drops product(s).
Consumers who have purchased Wellements Iron Drops with lot number coding of 18491 BB 1/2021 or Lot 10592 BB 10/2020 are urged to return it to the place of purchase or contact Wellements directly for a full refund. Consumers who received the promotional Iron Drops Sample with lot number coding of 10592 BB 10/2020 are urged to contact Wellements and return it. Consumers with questions may contact the company between 8am-5pm PST at 800-255-2690.

Jamaican Tastee Patties, LLC Recalls Meat and Poultry Patty Products Produced without Benefit of Inspection

July 28, 2020

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WASHINGTON, July 28, 2020 – Jamaican Tastee Patties, LLC, a Miami, Fla. firm, is recalling approximately 60,457 pounds of meat and poultry patty products that were repackaged, relabeled and redistributed without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The firm also applied the mark of inspection of another federal establishment without proper authorization.
The baked and unbaked, frozen beef and chicken patty items were produced on various dates from September 2018 through July 2020. The following products are subject to recall:
•    18-oz. boxes containing 4 pieces of “AUTHENTIC Jamaican STYLE TASTEE Patties JERK CHICKEN TURNOVERS BAKED” with various sell-by dates represented on the label.
•    18-oz. boxes containing 4 pieces of “AUTHENTIC Jamaican STYLE TASTEE Patties BEEF TURNOVERS SPICY BEEF BAKED” with various sell-by dates represented on the label.
•    18-oz. boxes containing 4 pieces of “Jamaican STYLE TASTEE Patties TURNOVERS CURRY CHICKEN BAKED” with various sell-by dates represented on the label.
•    18-oz. boxes containing 4 pieces of “AUTHENTIC Jamaican STYLE TASTEE Patties BEEF TURNOVERS MILD BEEF BAKED” with various sell-by dates represented on the label.
•    112-oz. (7-lb.) cases containing 24 pieces of “Authentic Jamaican STYLE TASTEE Patties BEEF TURNOVERS SPICY BEEF UNBAKED” with various sell-by dates represented on the label.
•    112-oz. (7-lb.) cases containing 24 pieces of “Authentic Jamaican STYLE TASTEE Patties BEEF TURNOVERS MILD BEEF UNBAKED” with various sell-by dates represented on the label.
The products subject to recall bear establishment number “EST. 2390” or “P-2390” inside the USDA mark of inspection. These items were shipped to retail and restaurant locations in Florida.
The problem was discovered during FSIS surveillance activities, which determined that the firm repackaged the beef and chicken patty products without the benefit of federal inspection and used the mark of inspection from another establishment without authorization.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS is concerned that some product may be in restaurant and consumers’ freezers. Restaurants that have purchased these products should not serve them. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Lance Williams, Owner, Jamaican Tastee Patties, LLC, at (305) 878-2716 or lanceprt@bellsouth.net.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Coco's Italian Market Recalls Italian Meatball, Beef Ravioli, and Pepperoni Pizza Products Produced without Benefit of Inspection

July 27, 2020

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WASHINGTON, July 24, 2020 - Coco's Italian Market, a Nashville, Tenn. establishment, is recalling approximately 16,868 pounds of various ready-to-eat frozen meat products that were produced without the benefit of federal inspection, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today.
The frozen Italian meatball, beef ravioli, and pepperoni pizza items were produced on various dates from January 2019 through July 2020. The following products are subject to recall: [View Labels (PDF only)]
•    16-oz. clear plastic bags packages containing 4 pieces of "Coco's ITALIAN MARKET Fully Cooked Italian Meatballs" and a USDA mark of inspection represented on the label.
•    15-oz. plastic-wrapped plastic covered containers containing "Coco's ITALIAN MARKET Take - n - Bake BEEF RAVIOLI WITH LUCIANA'S MARINARA SAUCE."
•    16-in. plastic-wrapped cardboard trays containing "Coco's ITALIAN MARKET Take - n - Bake Hand Made Pepperoni Pizza" with a USDA mark of inspection represented on the pepperoni label.
•    7-in. plastic-wrapped cardboard trays containing "Coco's ITALIAN MARKET Take - n - Bake Hand Made Pepperoni Pizza" with a USDA mark of inspection represented on the pepperoni label.
The products subject to recall do not bear an establishment number inside the USDA mark of inspection. These items were shipped to retail locations in Tennessee.
The problem was discovered when the Tennessee Department of Agriculture observed products produced by Coco's Italian Market in retail locations labeled with the federal marks of inspection. They also identified other labeling issues, such as the omission of net weight on the pepperoni pizza product.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers' freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Chuck Cinelli, Owner, Coco's Italian Market, at (615) 573-2319 or chuck.cinelli@gmail.com.

Real Clean Distribuciones SA de CV Issues Voluntary Nationwide Recall of Four Hand Sanitizer Due to Potential Presence of Undeclared Methanol (Wood Alcohol)

July 24, 2020

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La Loma, Tlalnepantla, Mexico, Real Clean Distribuciones SA de CV is voluntarily recalling all lots it manufactured within expiry of the following brand names of hand sanitizers:
•    Born Basic ANTI-BAC HAND SANITIZER,
•    Scent Theory KEEP CLEAN Moisturizing Hand Sanitizer,
•    Scent Theory KEEP IT CLEAN Moisturizing Hand Sanitizer, and
•    Lux Eoi Hand Sanitizing Gel to the consumer level.
The products are being recalled due to the potential presence of methanol (wood alcohol).
Risk Statement: Substantial methanol exposure could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, Real Clean Distribuciones SA de CV has not received reports of adverse events related to this recall.
RECALLED PRODUCTS
These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. Real Clean Distribuciones SA de CV manufacturers product for four brands included in this recall.
Scent Theory and Born Basic hand sanitizer products are produced by several different manufacturers, in several different countries, and only those lots manufactured by Real Clean in Mexico are subject to the recall.
The recalled products include the following lots:
Manufacturer    Product    Country of Origin    Size    Lot Numbers
Real Clean Distribuciones S.A. De C.V.    Scent Theory Keep Clean Hand Sanitizer 70% Alcohol    Mexico    16.9oz    1633220, 1733220, 1833220, 1933220, 2033220, 2133220, 2233220, 2333220, 2433220, 2533220, 2633220, 2733220, 2833220, 2933220, 3033220, 3133220, 3233220, 3333220, 3433220, 3533220, 3633220, 3733220, 3833220, 3933220, 4033220, 4133220
Real Clean Distribuciones S.A. De C.V.    Keep it Clean Hand Sanitizer 70% Alcohol    Mexico    16.9oz    0133220, 0233220, 0333220, 0433220, 0533220, 0633220, 0733220, 0833220, 0933220, 1033220 1133220, 1233220, 1333220, 1433220, 1533220
Real Clean Distribuciones S.A. De C.V.    Born Basic Anti-Bac Hand Sanitizer 70% Alcohol    Mexico    16.9oz    0833420, 0933420, 1033420, 1133420, 1233420, 1333420, 1433420, 1533420, 1633420, 1733420, 1833420, 1933420, 2033420, 2133420, 2233420, 2333420, 2433420, 2533420, 2633420, 2733420, 2833420, 2933420
Real Clean Distribuciones S.A. De C.V.    Born Basic Anti-Bac Hand Sanitizer 70% Alcohol    Mexico    34oz    0133420, 0233420, 0333420, 0433420, 0533420, 0633420
Real Clean Distribuciones S.A. De C.V.    Born Basic Anti-Bac Hand Sanitizer 70% Alcohol    Mexico    9.5oz    0133720, 0233720
Real Clean Distribuciones S.A. De C.V.    Lux Eoi Hand Sanitizing Gel    Mexico    16.9oz    0133920, 0233920, 0333920
Real Clean Distribuciones SA de CV is notifying its distributors by recall letter and consumers via this press release. Real Clean Distribuciones SA de CV is arranging for the return and refund of all recalled products.
Consumers/distributors/retailers that have the product subject to this recall should stop using/distributing/selling Hand Sanitizer and return it to the place of purchase; because the affected products are considered hazardous materials, do not destroy the affected products.
Consumers with questions regarding this recall can contact Stericycle during the following hours: Sunday - Saturday 08:00 am - 8:00 pm EST at:
•    Toll Free: 866-512-4073
•    FAX: 844-294-7183
•    Email: Realclean4107@stericycle.com

UpSpring LLC Issues Allergy Alert On Undeclared Milk In " UpSpring Baby Iron + Immunity "

July 24, 2020

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UpSpring LLC of Austin, TX is recalling one batch of its 60 ml dark brown glass bottles sold in cartons of "UpSpring Baby Iron + Immunity" dietary supplements because it may contain undeclared milk allergen. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.
UpSpring Baby Iron + Immunity dietary supplements were distributed nationwide via UpSpringBaby.com, Amazon.com and Target as well as in other retail stores and online channels between May 02, 2019 and July 17, 2020.
The recalled product comes in a 60 ml dark brown glass bottle within a carton with lot # 06691 and with an expiration date of March 2021. The lot # and expiration date can be located on the bottom of the carton in black ink and at the bottom of the glass bottle in yellow ink.
No allergic reaction has been reported to date with this product.
The recall was initiated after it was discovered that a milk-containing ingredient was added to the formula and was distributed in packaging that did not reveal the presence of milk. Subsequent investigation indicates the problem was caused by an unintentional mixing of lactose used in the manufacturing of this product.
Production of the product has been suspended.
Consumers who have purchased the 60 ml packages of “UpSpring Baby Iron + Immunity " from lot # 06691 are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-512-828- 7988 (Monday-Friday 8am-4pm CST) or info@upspringbaby.com.

Hostess Brands, LLC Issues Voluntary Recall of Certain Hostess® Raspberry Zingers® Due to the Potential for Mold

July 24, 2020

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Hostess Brands, LLC (“Hostess Brands”) is voluntarily recalling certain Hostess® Raspberry Zingers® because the product may develop mold prior to the best by date.
This recall applies to the following Raspberry Zinger® products:
Product    Item UPC    Batch    Best By Date
Hostess Raspberry Zingers (Multi-Pack fresh)    888109110604    H061224000    08/26/2020
        H061324000    08/27/2020
        H061424000    08/28/2020
        H061524000    08/29/2020
Hostess Raspberry Zingers (Multi-Pack frozen)    888109110604    H061524000     
Hostess Raspberry Zingers (Single-Serve fresh)    888109010089    H061224000    08/26/2020
        H061324000    08/27/2020
        H061424000    08/28/2020
Hostess Raspberry Zingers (Single-Serve frozen)    888109010089    H061424000     
        H061524000     
Hostess Raspberry Zingers (Single-Serve grocery 3 count)    888109010089    H061224000    8/26/2020
The products were sold to mass merchandisers, grocery stores, distributors, dollar and discount stores, and convenience stores throughout the United States.
Consumers who have purchased the affected product are urged to discontinue consumption and contact the place of purchase about returning them for a full refund.
This recall does not affect any other Hostess Brands products.
Consumers with questions may contact 1-800-483-7253 Monday through Friday from 8:30 am to 4:30 pm Central Time.
Hostess Brands, LLC
Hostess Brands, LLC is headquartered in Lenexa, Kansas and operates bakeries in Emporia, Kansas, Chicago, Illinois, Columbus, Georgia, Indianapolis, Indiana and through its Voortman Cookies Limited subsidiary, Burlington, Ontario.
For more information about Hostess products and Hostess Brands, please visit hostesscakes.com. Follow Hostess on Twitter: @Hostess_Snacks; on Facebook: facebook.com/Hostess; on Instagram: Hostess_Snacks; and on Pinterest: pinterest.com/hostesscakes.

InHe Manufacturing, LLC and MHR Brands Issues Voluntary Nationwide Recall of Several Products Due to Potential Health Risk for Excess Lead

July 23, 2020

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This recall press release was issued by the firm on 06-23-2020 and is subsequently being posted by FDA at this time only to benefit the public for informational purposes.
Human Consumption (MHR Brands)
Tasty Drops – Berry Tincture, 1oz/300mg
FG003175
Tasty Drops – Berry Tincture, 1oz/500mg
FG003137 FG003174, FG003197, FG0057
Tasty Drops – Berry Tincture, 1oz/1500mg
FG003141, FG003202, FG003296
Tasty Drops – Natural Tincture, 1oz/500mg
FG003138, FG003248
Tasty Drops – Natural Tincture, 1oz/1500mg
FG003142, FG003247
Tasty Drops – Spearmint Tincture, 1oz/300mg
FG003167
Tasty Drops – Spearmint Tincture, 1oz/500mg
FG003139, FG003166, FG003191, FG003225, FG003253, FG003263
Tasty Drops – Spearmint Tincture, 1oz/1000mg
FG003095
Tasty Drops – Spearmint Tincture, 1oz/1500mg
FG003143, FG003180, FG003201, FG003224, FG003262
Tasty Drops – Vanilla Tincture, 1oz/300mg
FG003126
Tasty Drops – Vanilla Tincture, 1oz/500mg
FG003140, FG003182, FG003246
Tasty Drops – Vanilla Tincture, 1oz/1500mg
FG003144, FG003249
Made by Hemp – French Vanilla Tincture, 1oz/1000mg
FG003107
Made by Hemp – Mojito Lime Tincture, 1oz/1000mg
FG003110
Made by Hemp – Strawberry Crème Tincture, 1oz/1000mg
FG003109
Pet Consumption (MHR Brands)
Tasty Drops – Cat Tincture 1oz/200mg
FG003156, FG003325
Tasty Drops – Dog Tincture 1oz/200mg
FG003157, FG003286, FG003324
Purfurred – Dog Tincture, 1oz/200mg
FG003188
Made by Hemp – Cat Tincture, 1oz/200mg
FG003178
Made by Hemp – Dog Tincture, 1oz/200mg
FG003179
Human Consumption (White Label)
A Clean Choice – French Vanilla Tincture, 1oz/1000mg
FG003106
A Clean Choice – Strawberry Creme Tincture, 1oz/1000mg
FG003108
A Clean Choice – Spearmint Tincture, 1oz/500mg
FG003113
BC Hemp Co LLC – Berry Tincture, 1oz/500mg
FG003312
BC Hemp Co LLC – Natural Tincture, 1oz/500mg
FG003171, FG003183, FG003316
BC Hemp Co LLC – Spearmint Tincture, 1oz/500mg
FG003315
BC Hemp Co LLC – Berry Tincture, 1oz/1000mg
FG003164
BC Hemp Co LLC – Natural Tincture, 1oz/1000mg
FG003318
Goodness Gurus – Berry Tincture, 1oz/500mg
FG003236
Goodness Gurus – Spearmint Tincture, 1oz/500mg
FG003234
Goodness Gurus – Spearmint Tincture, 1oz/1000mg
FG003238
Goodness Gurus – Spearmint Tincture, 1oz/1500mg
FG003237
Herbzeedy LLC – Natural Tincture, 1oz/500mg
FG003122, FG003123
Herbzeedy LLC – Natural Tincture, 1oz/1500mg
FG003121
Javan Anti Aging – Spearmint Tincture, 1oz/300mg
FG003283
Pathway to Wellness – Natural Tincture, 1000mg/30ml
FG003151
The Spiffy Piff – Berry Tincture, 1oz/300mg
FG003277
The Spiffy Piff – Spearmint Tincture, 1oz/300mg
FG003276
Recovery ReLeaf – Vanilla Tincture, 1oz/1000mg
FG003133
Acadia Farms – Canadian Maple Tincture, 1oz/300mg
FG003181
Acadia Farms – Spearmint Tincture, 1oz/300mg
FG003177
Pet Consumption (White Label)
Herbal Renewals – Cat Tincture, 1oz/200mg
FG003213
Herbal Renewals – Pet Blend, 1oz/200mg
FG003223, FG003310
Barkley Bistro – Dog Tincture, 1oz/200mg
FG003145
A Clean Choice – Cat Tincture, 1oz/200mg
FG003117
A Clean Choice – Cat Tincture, 500mg/1oz.
FG003118
A Clean Choice – Dog Tincture, 1oz/200mg
FG003116
A Clean Choice – Dog Tincture, 500mg/1oz.
FG003115
BC Hemp Co LLC – Pet Tincture, 1oz/200mg
FG003165
Boost IV Hydration, LLC – Dog Tincture, 1oz/200mg
FG003270
Acadia Farms – Pet Blend, 1oz/200mg
FG003176
How the company learned of this situation: The Company was recently advised by the Florida Department of Health of the presence of elevated heavy metals (lead) in some of its products. In response to this information, the Company undertook an investigation and determined that the issue related to graduated droppers provided by a third-party packaging supplier.
Exposure to lead could present physical signs and symptoms including, pain, paresthesia/muscle weakness, abdominal pain, nausea, vomiting, diarrhea, constipation, poor appetite, weight loss, symptoms associated with encephalitis, metallic taste in the mouth, shock, hemolysis or kidney damage.
In response and in conjunction with the regulatory authorities, the Company:
1.    issued a voluntary nationwide recall of the affected products, providing every customer with replacement products at no cost to the customer; and
2.    retained a replacement third-party packaging supplier for all replacement and future products.
3.    Discontinue use of graduated droppers in the future.
Prior to notifying customers of this recall, MHR Brands had not received any reports of adverse health effects regarding the recalled products. Consumers should contact their physician or healthcare provider if they experience any symptoms that may be related to using the products being recalled. Consumers should observe pets and contact their veterinarian as signs and symptoms of lead exposure in pets may be similar to those in humans.
Immediately examine your inventory and quarantine product subject to this recall. In addition, if you may have further distributed this product, please identify your customers and notify them at once of this product recall. Your notification to your customers should include a copy of this recall notification letter.
Product Disposition: Return the product to the Company or destruction.
This recall should be carried out to the consumer level. Your assistance is appreciated and necessary to complete this recall.
MHR distributes nationally directly to consumers thorough internet sales and is currently notifying all customers about the ongoing recall directly. The Company also manufactures for other marketers and is notifying those customer of this issue and the identified LOTS urging return of the product to the Company or place of purchase for a free replacement or to contact MHR Brands at 844-300-5673 Mon.-Fri. 9am-5pm (EST) or by email at recall@mhrbrands.com.
While this recall is being made with the knowledge of the Food and Drug Administration, FDA does not endorse any products subject to this recall notice.
Media Contact: Members of the media can contact the Company at 954-773-9456.

LIQ-E S.A. de C.V. Issues Voluntary Recall of the Optimus Instant Hand Sanitizer Due to the Potential Presence of Undeclared Methanol

July 20, 2020

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SAN NICOLAS DE LOS GARZA, Mexico -- LIQ-E S.A. de C.V. is voluntarily recalling all lots and all bottle sizes of The OPTIMUS Instant Hand Sanitizer due to the potential presence of methanol (wood alcohol) that were shipped into the United States. The products were manufactured between April 27, 2020 and May 08, 2020.
Risk Statement: Substantial methanol exposure could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, and permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, LIQ-E S.A. de C.V. has not received any reports of adverse events related to this recall.
Recalled Products
Product(s)    NDCs    Sizes    UPC    Lot #s & Expiration Dates
Optimus Instant Hand Sanitizer    75416-002-01    8.5Fl Oz.(250 mL)    7501799115621    (L) 20-02 EXP 05/2022
Optimus Instant Hand Sanitizer    75416-001-04    55 Gal (208 L)    7501799118998    See List
Optimus Instant Hand Sanitizer    75416-378-04    1 GAL (3.78L)    7501799118837    (L) 20-03 EXP 05/22
Optimus Instant Hand Sanitizer    75416-004-01    275 Gal (1,040 L)    7501799118981    (L) 5200 EXP 05/2022
55 Gal Blue Drum Lot Numbers:
L-1160 EXP 05/2022    L-2160 EXP 05/2022    L-3160 EXP 05/2022    L-1180 EXP 05/2022    L-2180 EXP 05/2022    L-2190 EXP 05/2022
L-1200 EXP 06/2022    L-2200 EXP 06/2022    L-3200 EXP 06/2022    L-4200 EXP 06/2022    L-5200 EXP 06/2022    L-1210 EXP 06/2022    L-2210 EXP 06/2022
Master Cartons Lot Numbers,
L-1150    L-2150    L-3150    L-4150    L-5150    L-6150
L-1160    L-2160    L-3160    L-4160    L-5160    L-6160
L-1170    L-2170    L-3170    L-4170    L-5170    L-1180
L-3180    L-4180    L-6180    L-1190    L-2190    L-3190
L-4190    L-5190    L-6190    L-1200    L-2200    L-3200
L-4200    L-5200    L-6200    L-2180        
The Hand Sanitizer is distributed in a 55 Gal (208 L) plastic blue drum and in 8.5Fl Oz. (250 mL), 1Gal (3.78 L), and 275 Gal (1,040L) clear plastic HDPE bottles or tank. All are labeled with a green and white label. The product was distributed throughout the United States.
Each product contains a lot number consisting of a letter followed by a dash four digits (example L-1180). This number can be found on the master cartons and written in black pen on the 55 Gal blue drum and the 275 Gal plastic tank.
The individual bottles are labeled with a lot number and expiration date in the format below. See table for lot numbers of each individual bottle.
(L) 20-02 EXP 05/2022
LIQ-E S.A. de C.V. is notifying its customers/distributors by recall letter and consumers via this press release. LIQ-E S.A. de C.V. is arranging for return and refund, if it is the case, of all recalled products.
Consumers/distributors/retailers that have the product subject to this recall should stop using/distributing the Optimus Instant Hand Sanitizer and return it to the place of purchase.
Consumers with questions regarding this recall can contact LIQ-E S.A. de C.V. during business hours: 9:00am – 5:00pm (CT)
Toll Free: 5281 81316021
FAX: 5281 81316018
Email: Ignacio.ortiz@liqesa.com

Giant Eagle Recalls Dried Fruit Mix Due to Undeclared Allergens

July 18, 2020

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Giant Eagle, Inc. has issued a voluntary recall of Giant Eagle Dried Island Fruit Mix due to the possibility the product may contain undeclared Peanut, Almond, Milk and Soy allergens. Those who have an allergy or severe sensitivity to Peanut, Almond, Milk or Soy could experience a serious or life-threatening allergic reaction if they consume these products.
The impacted product has a “best by” date of January 15, 2021 and can be identified by the UPC 3003491435. The recalled item was sold in the produce department of the Carmel Market District in Indiana, the Edinboro Giant Eagle in Pennsylvania and select Giant Eagle and Market District locations in Ohio. To date, there are no reported illnesses associated with this recall.
Giant Eagle was made aware of the issue by a guest who purchased the product and the company has since learned that the cause was a packaging error made by the product manufacturer.
Customers who have purchased the affected product should dispose of it or return a qualifying receipt to their local Giant Eagle or Market District store for a refund. Customers with questions may call Giant Eagle Customer Care at 1-800-553-2324 Monday through Friday 9 a.m. to 9 p.m. EST.
In addition to this public communication regarding this recall, Giant Eagle initiated its consumer recall telephone notification process. The consumer recall process uses purchase data and consumer telephone numbers housed in the Giant Eagle Advantage Card database to alert those households that purchased the affected product and have updated telephone contact information in the database.

KIND Issues Voluntary Recall Due to Undeclared Sesame Seeds in Oats & Honey

July 8, 2020

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KIND Healthy Snacks (KIND) is voluntarily recalling a limited number of Oats & Honey Granola with Toasted Coconut pouches due to the presence of sesame seeds, which is not listed as an ingredient in the product. The label does list “sesame seeds” under the “May Contain” statement.
People who have an allergy or sensitivity to sesame seeds should immediately discontinue use of this product. No allergic reactions have been reported to date. This product may be safely consumed by those who do not have an allergy or sensitivity to sesame seeds.
KIND recently decided to transition away from using sesame seeds in its Oats & Honey Granola recipe. This limited recall was initiated after KIND discovered that the product’s previous recipe was used and placed into new packaging that did not disclose sesame seeds as an ingredient.
The recall applies to one flavor: KIND Oats & Honey Granola with Toasted Coconut. No other KIND products are affected by this recall.
The product is sold in a plastic pouch and is available in two sizes – 11 ounces (UPC: 60265217186-4) or 17 ounces (UPC: 60265225101-6).
The impacted product can be identified by looking for the Best By date, which is located on the bottom of the pouch:
•    For the 11oz pouch, the Best By dates range from April 4, 2021 to June 1, 2021
•    For the 17oz pouch, the Best By dates range from April 30, 2021 to June 1, 2021
Please visit kindsnacks.com/oatsandhoneygranolaExternal Link Disclaimer for more information.
The product was manufactured in the United States and distributed through retail stores and ecommerce sites. This limited voluntary recall is being conducted in cooperation with the U.S. Food and Drug Administration.
Consumers who have purchased KIND Oats & Honey Granola that displays one of the abovementioned Best By Dates and can no longer consume the product safely due to an allergy or sensitivity to sesame seeds, should retain the packaging and email customerservice@kindsnacks.com.

Allergy Alert Issued by Winter Gardens Quality Foods, Inc. for Undeclared Egg in Spinach Artichoke Dip

July 17, 2020

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Winter Gardens Quality Foods, Inc., is voluntary recalling one of its products: Whole Foods Market Spinach Artichoke Dip carrying the lot code 248 and Use By: 07/26/20, because of an undeclared allergen (Egg). Consumers who have a food allergy or have severe sensitivity to Egg should not consume the product as it could result in a serious life-threatening allergic reaction. The lot code can be found printed on the lid.
The affected product was sold at Whole Foods Market stores in Pennsylvania, Maryland, Virginia, New Jersey and Washington DC on or after July 14, 2020. The product was located in refrigerated aisles in a 12 oz plastic tub and the incorrectly labeled items will have the following UPC code: 074204804467 and the labels below:
No illnesses have been reported to date.
The recall was initiated following an internal review of records identified the incorrect label.
Winter Gardens is cooperating fully with regulatory authorities to successfully return all suspected product and has taken substantial actions to prevent any recurrences.
Consumers with questions about the recall can contact us Monday through Friday from 8am – 4pm at the following contact:
David Mulligan, Winter Gardens Quality Manager at 717-624-6032

Happy Colon Foods, LLC Issues Allergy Alert on Undeclared Milk in Happy Colon Yum Shortbread Cookie and Happy Colon Mmmm Chocolate Chip Cookie

July 17, 2020

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Happy Colon Foods, LLC of Oklahoma City, Oklahoma is recalling Happy Colon YUM Shortbread Cookie and Happy Colon Mmmm Chocolate Chip Cookie, because they may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume this product.
Happy Colon YUM Shortbread Cookies and Happy Colon Mmmm Chocolate Chip Cookies were distributed in Oklahoma, New York, Connecticut, Texas, North Carolina, Kansas, Pennsylvania, New Jersey, Tennessee, Arizona via mail order and direct delivery.
Happy Colon YUM Shortbread Cookies and Happy Colon Mmmm Chocolate Chip Cookies are packaged in white film and are distributed within the Happy Colon Foods prep kit. Affected product has an expiration date Sept. 27, 2020. Net weight 0.98 oz (28g).
No illnesses have been reported to date.
The recall was initiated after it was discovered that Happy Colon YUM Shortbread Cookies and Happy Colon Mmmm Chocolate Chip Cookies containing milk were distributed in packaging that did not reveal the presence of milk. Subsequent investigation indicates the problem was caused by a printing error on labeling.
Consumers who have purchased Happy Colon Foods kits prior to July 15, 2020 may contact the company at 1-855-423-6637 Mon-Fri 8am – 5pm CST. Households with individuals that have an allergy or sensitivity to milk should dispose of the recalled product.

4e Brands North America Issues Nationwide Voluntary Recall of Hand Sanitizer Due to Potential Presence of Undeclared Methanol (Wood Alcohol)

July 14, 2020

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San Antonio, Texas, 4e Brands North America is voluntarily recalling ten (10) bottle sizes of Hand Sanitizers to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol).
Risk Statement: Substantial methanol exposure could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, 4e Brands North America has not received reports of adverse events related to this recall.
Recalled Products
These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. The affected Hand Sanitizers are packaged in clear plastic bottles. The recalled products are as follows (a full listing of lot numbers in numerical order is included below the chart):
Product(s)    NDC(s)    SIZE    UPC    LOT

BLUMEN Advanced Instant Hand Sanitizer
Clear    60599-015-00    33.8 fl oz / 1L    814266023747    2213, 2219, 2220, 2221, 2223, 2225, 2252, 2255,
2226, 2227, 2254, 2467,
2244, 2247, 2229, 2845,
2847, 2212, 2217, 2222,
2250, 2249, 2463, 2465,
2676, 2678, 2846, 2216,
2228, 2399, 2464, 2466,
2684, 2246, 2259, 2675,
2683, 2218, 2245, 2231,
2258, 2202, 2215, 2224,
2441, 2251, 2230, 2681,
2256, 2257, 2679, 2682

BLUMEN Advanced Hand Sanitizer    

60599-012-04    7.5 fl oz/ 221 ml    814266023624    2369, 2440, 2368, 2499,
2439, 2576, 2680, 2744,
2498, 2968, 2497
    60599-012-08    33.8 fl oz / 1L    814266023693    2833, 2748, 2844, 2838,
2775, 2750, 2837, 2839,
2836, 2786, 2905, 2897,
2898, 2907, 2896, 2899,
2906, 2908, 2997, 2372,
2894, 2895, 2374, 2373,
2909

BLUMEN Clear LEAR Advanced Hand Sanitizer    60599 -017-00    18 fl oz / 532 ml    814266023914    2910 , 2753
    60599-018-01    2 fl oz / 60 ml    814266023716    2234, 2571, 2383

BLUMEN Clear Advanced Hand Sanitizer    60599-018-02    7.5 fl oz / 221 ml    814266023624    2743, 2507, 2459, 2543,
2797, 2799, 2461, 2542,
2800, 2802, 2601, 2361,
2546, 2371, 2544, 2462, 2573, 2574, 2670, 2671,
2787, 2891, 2998, 2140,
2265, 2804, 2889, 2438,
2400, 2401, 2382, 2504,
3007, 2128, 2131, 2266,
2365, 2458, 2460, 2773,
2512, 2296, 2133, 2352,
2364, 2457, 2545, 2883,
2969, 2268, 2243, 2878,
2363, 2134
    60599-018-04    17 fl oz / 503 ml    814266024096    2263, 2362, 2367, 2780,
2269, 2264, 2741, 2749,
2366, 2745, 2778, 2188,
2293, 2294, 2132, 2135,
2669, 2501, 2673, 2505,
2885, 2788, 2877, 2879,
2187, 2130, 2261, 2262,
2600, 2500, 2509, 2515,
2752, 2876, 2351, 2295, 2297, 2575, 2834, 2514,
2890, 2129, 2136, 2832,
2506, 2508, 2892, 2911,
2742, 2502, 2503, 2831,
2779, 2511, 2835, 2740,
2776, 2513, 2785, 2516,
2267
    60599-018-06    1.05 GAL / 4L    814266023686    2887, 2888, 2672, 2746,
2510, 2886, 2884, 2602,
2747, 2830, 2777, 2518,
2774, 2801, 2781, 2798,
2784, 2805
    60599-018-07    3.4 fl oz 100 ml    814266023594    2360, 2370, 2531, 2567,
2141, 2967, 2843, 2880,
2253
BLUMEN Aloe Advanced Hand Sanitizer, with 70 Alcohol    

60599-028-00;    3.4 fl oz / 100 ml    814266023587    2369, 2440, 2368
LOT NUMBERS
2128    2226    2267    2400    2510    2678    2787    2885
2129    2227    2268    2401    2512    2679    2788    2886
2130    2228    2269    2438    2513    2680    2797    2887
2131    2229    2293    2439    2514    2681    2799    2888
2132    2230    2294    2440    2515    2682    2801    2889
2133    2234    2295    2441    2518    2683    2804    2890
2134    2243    2296    2457    2531    2684    2805    2891
2135    2244    2297    2458    2542    2740    2830    2892
2136    2245    2351    2459    2543    2741    2832    2894
2140    2246    2352    2460    2544    2743    2833    2895
2141    2247    2360    2461    2546    2744    2834    2896
2187    2249    2361    2462    2567    2746    2835    2897
2188    2250    2362    2463    2571    2747    2836    2898
2202    2251    2363    2464    2573    2748    2837    2899
2212    2252    2364    2465    2574    2749    2838    2905
2213    2253    2365    2466    2575    2750    2839    2906
2215    2254    2366    2467    2576    2752    2843    2907
2216    2255    2367    2497    2600    2753    2844    2908
2217    2256    2368    2499    2601    2773    2845    2909
2218    2257    2369    2500    2602    2774    2846    2910
2219    2259    2370    2501    2669    2775    2847    2911
2220    2261    2371    2504    2670    2776    2876    2969
2221    2262    2372    2505    2671    2777    2877    2998
2222    2263    2374    2506    2672    2780    2878    3007
2223    2264    2382    2507    2673    2781    2879     
2224    2265    2383    2508    2675    2784    2880     
2225    2266    2399    2509    2676    2785    2884     
The Hand Sanitizer is in a clear bottle with a blue cap. The product label contains only blue, white, silver, and red coloring. The lot number is four digits and printed on the bottle. The product was distributed nationwide in the United States through retailers and distributors. 4e Brands North America is notifying its distributors and retailers by recall letter and consumers via this press release. 4e Brands North America is arranging for the return and refund of all recalled products.
Consumers/distributors/retailers that have the product subject to this recall should stop using/distributing/selling Hand Sanitizer and return it to the place of purchase.
Consumers with questions regarding this recall can contact 4e Brands North America LLC during business hours: Monday - Friday 08:00 am - 5:00 pm EST at:
Toll Free: 888-843-0254
FAX: 888-214-7430
Email: 4EBrands8797@stericycle.com Event 8797
Consumers should contact their physician or healthcare provider if they experienced any problems that may be related to taking or using this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

C.V. Issues Voluntary Nationwide Recall of all Lots Within Expiry of bio aaa Advance Hand Sanitizer 480 mL Due to the Potential Presence of Undeclared Methanol (Wood Alcohol)

July 14, 2020

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AAA Cosmética, S.A. de AAA Cosmética, S.A. de C.V. is voluntarily recalling all lots of bio aaa Advance Hand Sanitizer currently in US distribution, packaged in 480 mL bottles, to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol).
Risk Statement: Substantial methanol exposure could result in nausea, diarrhea, vomiting, severe abdominal pain, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Persons using these products on their hands may be at risk; however young children who accidently ingest them and adolescents and adults who drink these products are most at risk for methanol poisoning. To date, AAA Cosmética has not received any complaints or adverse event reports related to this recall.
The product is used as a hand sanitizer and it is packaged in 480 mL plastic bottles.  AAA Cosmetica is recalling the following bio aaa Advance Hand Sanitizer lots, all of which bear the expiration date of April 2022:
20DF9001    20DF9002    20DF9003    20DF9004    20DF9005    20DF9006
20DF9007    20DF9008    20DF9009    20DF9010    20DF9011    20DF9012
20DF9013    20DF9014    20DF9015    20DF9016    20DF9017    20DF9018
20DF9019    20DF9020    20DF9021    20DF9022          
The product can be identified by the images. Product was distributed Nationwide in the United States beginning in April 2020.
AAA Cosmetica has notified its distributor, who will help notify its customers by phone calls, emails, and letters. AAA Cosmetica is arranging for refund and destruction of recalled products. Consumers/distributors/retailers that have the above listed lots of bio aaa Hand Sanitizer should stop using or distributing the products immediately and mail the products to AAA Cosmetica at the address below for refund:
I.S.C. Forwarder Inc.
8400 San Lorenzo,
Laredo, Texas 78045
(956) 753 0225
Consumers with questions regarding this recall can contact AAA Cosmética by phone +525526281124 or e-mail to customerservice@aaacosmetica.com.mx Monday to Friday from 10:00 am to 5:00 pm Central Time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Flagstone Foods, LLC. Issues Voluntary Recall of Wegmans Pecan Blend Due to Undeclared Almonds and Walnuts

July 13, 2020

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Flagstone Foods LLC, of Robersonville, NC, is recalling its 16-ounce packages ofWegmans Pecan Blend Trail Mix because they may contain undeclared almonds and walnuts. The product comes in a 16-ounce, plastic stand-up resealable package, marked with UPC Code 0-77890-31040-3 and lot code #05M04300 on the bottom right-hand side of the package with a Best By JAN 29 2021. People who are allergic to almonds or walnuts run the risk of a serious or life-threatening allergic reaction if they consume these products.
No illnesses or injuries have been reported to date.
The recalled Wegmans Pecan Blend packages were distributed to retail stores in Maryland, Massachusetts, New York, New Jersey, North Carolina, Pennsylvania and Virginia. Flagstone Foods is initiating the voluntary recall out of an abundance of caution to protect public health.
The recall was initiated after a customer notified the firm that the product contained almonds and walnuts that are not listed in the ingredient statement on the packaging.
Consumers who have purchased 16-ounce packages of Wegmans Pecan Blend Trail Mix with the above lot code and expiration date are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-612-222-3857 Monday – Friday 8:00 am – 6:00 pm CST.

ITECH 361 Issues Voluntary Nationwide Recall of All Clean Hand Sanitizer and Moisturizer and Disinfectant Due to The Potential Presence of Undeclared Methanol (Wood Alcohol)

July 6, 2020

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ITECH 361 is voluntarily recalling 18,940 bottles of All Clean Hand Sanitizer, Moisturizer and Disinfectant sold in one liter bottles to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol).
Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning To date ITECH 361 has not received reports of adverse events related to this recall.
The product is used as a hand sanitizer and moisturizer and is packaged in one (1) liter plastic bottles with UPC Code 628055370130. All Clean Hand Sanitizer and Moisturizer was distributed Nationwide to wholesale distributors and retailers.
ITECH 361 is notifying its distributors by a Notice of a voluntary recall and consumers via this press release. ITECH 361 is arranging for return/replacement or refund of all recalled products.
Consumers/distributors/retailers that have the product subject to this recall should stop using All Clean Hand Sanitizer, Moisturizer and Disinfectant and return it to the place of purchase.
Consumers with questions regarding this recall can contact Corina Enriquez by phone number (888)405-4442 or e-mail at corina@itech361.com, Monday through Friday beginning July 6, 9:00a.m. to 5:00 p.m. (MDT). Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

The J. M. Smucker Company Issues Voluntary Recall of One Lot of Natural Balance® Ultra Premium Chicken & Liver Paté Formula Canned Cat Food

July 3, 2020

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The J. M. Smucker Company today announced a voluntary recall of one lot of Natural Balance® Ultra Premium Chicken & Liver Paté Formula canned cat food due to health concerns likely associated with elevated levels of choline chloride.
Ingesting impacted product may cause nausea with excessive salivation, constricted pupils and poor vision, diarrhea or vomiting to more severe symptoms including difficulty walking, muscle shaking, tremors, irregular heartbeat, difficulty breathing, possible cardiac or respiratory failure and, in extreme situations, death. Pet parents are encouraged to contact their cat’s veterinarian immediately if their cat is displaying any of these symptoms.
If pet parents have any product matching the following description in their possession, they should stop feeding it to their cats and dispose of the product. This information can be found on the bottom of each can.
Product Name    Retail UPC Code    Lot Code    Best If Used By Date
Natural Balance® Ultra Premium Chicken & Liver Paté Formula canned cat food
5.5 oz can    2363353227    9217803    08 04 2021
These products are most commonly sold in pet specialty retailers and online throughout the United States and Canada. No other Natural Balance® products are impacted by this recall.
The Company has received reports of adverse reactions. Pet parents that have questions or would like to report adverse reactions should call 888-569-6828, Monday through Friday, 8 a.m. – 5 p.m. ET or email anytime at info@naturalbalanceinc.com.
This recall is being conducted in cooperation with the U.S. Food and Drug Administration.

Garland Ventures LTD Voluntary Recalls Five Cheese Stuffed Shells Because of Possible Health Risk

July 2, 2020

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Garland Ventures Ltd of Garland, Texas is voluntary recalling 1095 cases of Five Cheese Stuffed Shells trays because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled “Five Cheese Stuffed Shells” was distributed nationwide in limited number of retail stores.
The product “Five Cheese Stuffed Shells” comes in 10.76 ounces containing shells with marinara sauce, mozzarella cheese and parsley, and packed in aluminum foil container with clear lid marked lot# F080SS/F090SS on the bottom of label.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after samples tested through certified laboratory revealed the presence of Listeria monocytogenes in “Five Cheese Stuffed Shells”. Garland Ventures Ltd ceased the further production and distribution of product immediately.
Consumers who have purchased 10.76 ounce trays of “Five Cheese Stuffed Shells” are urged to return them to the place of purchase for full refund. Consumers with questions may contact Bob Cocat anytime at 972-795-5313.

Norpac Fisheries Export Recalls Shrimp Poke Due to Possible Health Risk

July 2, 2020

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Norpac Fisheries Export is recalling all fresh shrimp poke distributed in the Hawaiian Island between May 11, 2020 and June 25, 2020 because it has potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Product was distributed in Hawaii on The Big Island, Maui, Oahu, and Kauai through its retail customers, specifically Safeway Stores.
Any fresh shrimp poke purchased from their stores from May 11th, through June 25, 2020 would be potentially contaminated.
Shrimp poke is distributed as pre-mixed in plastic pouches and go to service counter and then dishes out in various weight increments into a “deli cup”. This is a photo of product and label.
"No illnesses have been reported to date."
We became aware of this problem during our routine Food Safety monitoring procedures, as we perform laboratory analysis of our work areas, equipment, surfaces, drains, raw materials and completed product. As a result of our routine random product and materials testing, we tested the shrimp used to make the shrimp poke, by having a sample sent to an independent lab for analysis. The results were received June 25, 2020 indicating a positive result for Listeria monocytogenes. We are proceeding under the cautious assumption that all of the shrimp from our supplier is contaminated.
Our company has ceased the production and distribution of the product using this shrimp, as the FDA and the company continue their investigation as to the exact source of the problem.
Consumers who have purchased Fresh Shrimp Poke are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1-808-842-3474 Mon – Fri 8:00am. – 5:00pm. (HST, Hawaii standard time).

Mount Franklin Foods, LLC dba Azar Nut Company Issues Allergy Alert on Undeclared Peanuts in “7-Select Yogurt Pretzels”

June 23, 2020

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Mount Franklin Foods, LLC dba Azar Nut Company of El Paso, TX is voluntarily recalling its 5-ounce packages of "7-Select Yogurt Pretzels" because they may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life- threatening allergic reaction if they consume these products.
The recalled 5-ounce packages of "7-Select Yogurt Pretzels" were distributed nationwide in retail 7-Eleven stores.
The product comes in a 5 ounce, printed plastic pouch and is marked with lot number YR20140 Best By May/19/2021 and JT20147 Best By May/26/2021 on the bottom front left of the bag.
No illnesses have been reported to date in connection with this alert.
The recall was initiated after discovering a peanut-containing product mixed with pretzels from a third-party supplier during the repackaging process of the "7-Select Yogurt Pretzels" which does not include peanuts in the declared allergens. Subsequent investigation indicates the problem was caused by an isolated incident whereby inclusion occurred during the sample inspection process.
Production of the "7-Select Yogurt Pretzels” has been suspended until FDA and the company are certain that the problem has been corrected.
Consumers who have purchased 5-ounce packages of "7-Select Yogurt Pretzels" with the above indicated lot numbers printed, are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-351-8178, M-F 8am – 5pm MT.

ALDI Voluntarily Recalls Little Salad Bar Garden Salad

June 23, 2020

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In cooperation with Fresh Express Inc., and out of an abundance of caution, ALDI has removed Little Salad Bar Garden Salad from select stores as a precautionary measure due to possible Cyclospora infection.
The recall affects all product codes of ALDI Little Salad Bar Garden Salads with use-by dates of May 16 to July 04 and distributed in the states of Arkansas, Illinois, Iowa, Indiana, Michigan, Minnesota, Missouri, North Dakota, South Dakota and Wisconsin between May 1 and June 19.
If customers have the affected Little Salad Bar Garden Salad, they should discard it immediately.
Customers with additional questions can contact Fresh Express Consumer Response Center toll-free at (800) 242-5472 Monday - Friday during the hours of 8 a.m. to 7 p.m. Eastern time.

Flagstone Foods, LLC. Issues Voluntary Recall of North Star Sweet & Salty Caramel Trail Mix Due to Undeclared Allergen

June 23, 2020

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Flagstone Foods LLC, of Robersonville, NC, is recalling its 14-ounce packages of North Star Sweet & Salty Caramel Trail Mix because they may contain undeclared cashews. The product comes in a 14-ounce, plastic stand-up resealable package, marked with UPC Code 0- 80948-63064-4 and lot code # 05M04210 on the bottom right-hand side of the package with an expiration date of 04/22/2021. People who are allergic to cashews run the risk of a serious or life-threatening allergic reaction if they consume these products.
The recalled North Star Sweet & Salty Caramel Trail Mix packages were distributed nationwide in retail military exchanges. No illnesses have been reported to date; however, Flagstone Foods is initiating the voluntary recall out of an abundance of caution to protect public health.
The recall was initiated after it was discovered that the cashew-containing product was distributed in packaging that does not disclose the presence of cashews.
Consumers who have purchased 14-ounce packages of North Star Sweet & Salty Caramel Trail Mix with the above lot code and expiration date are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Janet Collins, Director of Quality Assurance at 1-612-222-3857, Monday through Friday 8 am – 5 pm CST.

Hy-Vee Recalls 12 oz. Hy-Vee Garden Salad Product Per Supplier Notes of Potential Cyclospora Contamination

June 23, 2020

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Hy-Vee, Inc., based in West Des Moines, Iowa, is recalling its 12 oz. Hy-Vee Bagged Garden Salad product across its eight-state region due to the potential that it may be contaminated with Cyclospora. The potential for contamination was brought to Hy-Vee’s attention when Fresh Express – which manufactures the product – announced that the U.S. Food and Drug Administration (FDA) and the Centers for Disease Control Prevention (CDC) have been investigating an outbreak of Cyclospora in the upper Midwest section of the United States.
In their investigation, they have identified certain products linked to the outbreak – including Fresh Express’ private label products at retailers across the country that were impacted – including one for Hy-Vee. The recall is limited to 12 oz. Hy-Vee Bagged Garden Salad, all UPCs and expirations dates. The product was distributed to Hy-Vee grocery stores across its eight-state region of Iowa, Illinois, Missouri, Kansas, Nebraska, South Dakota, Minnesota and Wisconsin. No other Hy-Vee food items are impacted by this recall.
Hy-Vee has not received any reports of illness due to consumption of its Hy-Vee Bagged Garden Salad. Customers who purchased this product should discard it or return it to their local Hy-Vee store for a full refund.
Symptoms of cyclosporiasis begin an average of seven days after ingestion of Cyclospora. Symptoms of cyclosporiasis may include: watery diarrhea (most common), loss of appetite, weight loss, cramping, bloating, increased gas, nausea, fatigue, vomiting, and low-grade fever. If not treated, symptoms can persist for several weeks to a month or more. People who are in poor health or who have weakened immune systems may be at higher risk for severe or prolonged illness.
Consumers with questions may contact Hy-Vee Customer Care representatives 24 hours a day, seven days a week at 1-800-772-4098.

GSK Consumer Healthcare Issues Voluntary Nationwide Recall of Children's Robitussin® Honey Cough and Chest Congestion DM and Children's Dimetapp® Cold and Cough Due to Dosing Cups Missing Some Graduation Markings

June 18, 2020

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GSK Consumer Healthcare is voluntarily recalling to the retail level two lots (listed below) of Children's Robitussin® Honey Cough and Chest Congestion DM and one lot of Children's Dimetapp® Cold and Cough, due to the inclusion of incorrect dosing cups. During the review of the packaging documents for these products, GSK discovered that the dosing cups for the Children's Robitussin® Honey product are missing the 5 mL and 10 mL graduations, while the dosing cups for the Children's Dimetapp® product are missing the 10 mL graduation. The dosing cups packaged with both products only have the 20 mL graduation.
There is a potential risk of accidental overdose if caregivers dispensing the syrup do not notice the discrepancies between the graduations printed on the dosing cups and the indicated amounts to be administered (as directed in the instructions for use). Children's Robitussin Honey Cough & Chest Congestion DM contains 10 mg dextromethorphan HBr USP and guaifenesin USP 100 mg per 10 mL, and is labeled for children 4 and older, as well as adults. Children's Dimetapp Cold & Cough contains 2 mg brompheniramine maleate USP, 10 mg dextromethorphan HBr USP, and 5 mg phenylephrine HCl USP per 10 mL, and is labeled for children 6 and older, as well as adults. Symptoms of overdose of either product may include any of the following: impaired coordination; brain stimulation causing increase in energy, elevation in blood pressure, heart rate, and respiration; a lack of energy and enthusiasm; severe dizziness or drowsiness; slow heart rate; fainting; psychotic behaviour; restlessness; seizure; decreased respiration; nausea; vomiting; constipation; diarrhea; abdominal pain; visual and hearing hallucinations; urinary retention. As of the date of the recall announcement, GSK Consumer Healthcare has not received any adverse events related to these products or consumer complaints regarding the incorrect dosing cups supplied with the product.
The recall is limited to the three lots listed below:
Children's Robitussin® Honey Cough and Chest Congestion DM (4oz)
NDC 0031-8760-12
Lots: 02177 (Exp. Jan. 2022)
02178 (Exp. Jan. 2022)
Children's Dimetapp® Cold and Cough (8oz)
NDC 0031-2234-19
Lot: CL8292 (Exp. Sep. 2021)
These lots were distributed nationwide between February 5, 2020 and June 3, 2020 within the United States. GSK Consumer Healthcare has notified wholesalers, distributors and retailers to arrange for return of any recalled product. Wholesalers, distributors and retailers with an existing inventory of the lots being recalled should stop distribution and quarantine these lots immediately. Wholesalers, distributors and retailers that have further distributed the recalled product should notify any accounts or additional locations which may have received the recalled product from them.
Consumers with questions regarding this recall or to report an adverse experience please call 1-800-762-4675, Monday – Friday, 8:00am – 6:00pm EST.

Salad Supplier Recall Expanded after Potential Cyclospora Contamination; Hy-Vee Pulls Additional Salads as a Result

June 29, 2020

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Hy-Vee, Inc., based in West Des Moines, Iowa, is recalling an additional 12 salads across its eight-state region due to the potential that they may be contaminated with Cyclospora. The potential for contamination was brought to Hy-Vee’s attention when Fresh Express – which manufactures the product – announced that the U.S. Food and Drug Administration (FDA) and the Centers for Disease Control Prevention (CDC) expanded its investigation of an outbreak of Cyclospora in the upper Midwest section of the United States. The 12 salads are in addition to the 12 oz. Hy-Vee Bagged Garden Salad product that Hy-Vee pulled last week after initial notification of the investigation. Hy-Vee now has 13 private label bagged salad products (all expiration dates) that are being recalled as a result.
The products were distributed to Hy-Vee grocery stores across its eight-state region of Iowa, Illinois, Missouri, Kansas, Nebraska, South Dakota, Minnesota and Wisconsin.
The list below outlines the 13 products that have been recalled. No other Hy-Vee branded salads are impacted by today’s recall.
UPC    DESCRIPTION    SIZE
0-07450-24669    HY-VEE SOUTHWEST CHOPPED SALAD KIT    13.4 OZ
0-07545-12053    HY-VEE SHREDDED ICEBERG    8 OZ
0-75450-08530    HY-VEE VEGGIE DELUXE SALAD    12 OZ
0-75450-12046    HY-VEE GREENER SUPREME BLEND    12 OZ
0-75450-12047    HY-VEE AMERICAN BLEND SALAD    12 OZ
0-75450-12048    HY-VEE ITALIAN BLEND SALAD    10 OZ
0-75450-12051    HY-VEE COLESLAW MIX    16 OZ
0-75450-12058    HY-VEE ROMAINE GARDEN SALAD    12 OZ
0-75450-24668    HY-VEE ASIAN CHOPPED SALAD KIT    13.7 OZ
0-75450-24670    HY-VEE SUNFLOWER CHOPPED SALAD KIT    13.2 OZ
0-75450-24672    HY-VEE CHIPOTLE CHEDDAR CHOPPED KIT    11.4 OZ
0-75450-24674    HY-VEE GARDEN SALAD    12 OZ
0-75450-24715    HY-VEE AVOCADO RANCH CHOPPED KIT    12.8 OZ
Customers who purchased any of these products should discard them or return them to their local Hy-Vee store for a full refund.
Symptoms of cyclosporiasis begin an average of seven days after ingestion of Cyclospora. Symptoms of cyclosporiasis may include: watery diarrhea (most common), loss of appetite, weight loss, cramping, bloating, increased gas, nausea, fatigue, vomiting, and low-grade fever. If not treated, symptoms can persist for several weeks to a month or more. People who are in poor health or who have weakened immune systems may be at higher risk for severe or prolonged illness.
Consumers with questions may contact Hy-Vee Customer Care representatives 24 hours a day, seven days a week at 1-800-772-4098.
For more information, visit the FDA’s website at www.fda.gov.
Hy-Vee, Inc. is an employee-owned corporation operating more than 265 retail stores across eight Midwestern states with sales of $10 billion annually. The supermarket chain is synonymous with quality, variety, convenience, healthy lifestyles, culinary expertise and superior customer service. Hy-Vee ranks in the Top 10 Most Trusted Brands and has been named one of America’s Top 5 favorite grocery stores. The company’s 85,000 employees provide “A Helpful Smile in Every Aisle” to customers every day. For additional information, visit www.hy-vee.com.

UVT, INC. Issues Voluntary Nationwide Recall of SANIDERM ADVANCED HAND SANITIZER Due to the Potential Presence of Undeclared Methanol (Wood Alcohol)

June 29, 2020

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UVT, INC. is voluntarily recalling 38,830 liters of SANIDERM ADVANCED HAND SANITIZER, packaged in 1-liter bottles to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol)
Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, UVT, INC. has not received any reports of adverse events related to this recall.
The product is used as a hand sanitizer and is packaged in 1-liter plastic bottles. The affected SANIDERM ADVANCED HAND SANITIZER includes lot number 0530, Expiration date 04/2022. The product can be identified by the label below. Product was distributed Nationwide in the United States.
UVT, INC. is notifying its distributors and customers by phone calls, emails and letter and is arranging for replacement and destruction of all recalled products.
Consumers/distributors/retailers that have product which is being recalled should stop using products, initiate recalls to the user level, and return all products to the place of purchase. purchase.
Consumers with questions regarding this recall can contact UVT, INC. by phone (951) 427- 3108 or e-mail to customerservice@uvt.world Monday to Friday from 9:00 am and 3:00 pm Pacific Time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
•    Complete and submit the report Online
•    Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Fresh Express Issues a Precautionary Recall of Products Containing Iceberg, Red Cabbage and Carrots Produced at Its Streamwood, IL Facility Due to a Potential Cyclospora Risk

June 29, 2020

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Fresh Express, out of an abundance of caution, has issued a voluntary recall of branded and private label salad products produced at its Streamwood, IL facility that contain iceberg lettuce, red cabbage and/or carrot ingredients due to a possible health risk from Cyclospora. According to the Centers for Disease Control and Prevention, over 200 illnesses have been reported in connection with a current outbreak of Cyclospora occurring in primarily Midwest states.
Cyclosporiasis is an intestinal infection caused by the Cyclospora parasite. A person may become infected after ingesting contaminated food or water. Common symptoms include severe abdominal pain, diarrhea, nausea and vomiting, body aches and fatigue. The infection is treated with antibiotics and most people respond quickly to treatment.
The Fresh Express recall includes only those salads that are clearly marked with the letter Z at the beginning of the Product Code, which is located in the upper right-hand corner of the front of the package. Products containing the ingredients iceberg lettuce, red cabbage and/or carrots AND displaying the Product Code Z178, or a lower number, are recalled.
Recalled products were distributed to select retail stores between June 6 and June 26 in various states including, for example, Arkansas, Connecticut, Delaware, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Dakota, Tennessee, Virginia, Vermont, Wisconsin, West Virginia, and the District of Columbia.
No other Fresh Express products are subject to recall.
Fresh Express customers have been notified of the recall and instructed to immediately remove recalled products from all store shelves, distribution, and other inventories to ensure they are no longer available for sale or consumption.
Consumers who may have a recalled salad should discard it immediately and not eat it. Consumers with questions, or to obtain refunds, may contact the Fresh Express Consumer Response Center toll-free at (800) 242-5472 on Monday through Saturday from 8 a.m. to 7 p.m. Eastern time and on Sunday from 11 a.m. to 7 p.m. Eastern time.
Fresh Express takes food safety matters very seriously, stringently follows all mandated regulations and implements preventive measures designed to minimize potential risks. Fresh Express is working in close coordination with FDA in its continuing investigation to identify a definitive source of the current Cyclospora outbreak.
Recalled Product Details

Fresh Express Precautionary Recall 06/27/2020
Streamwood IL Facility-Produced Salads Containing Iceberg Lettuce, Red Cabbage or Carrots AND Product Code
of Z178 or a Lower Number
(No other Fresh Express salads are included in this recall)
BRAND/PRODUCT NAME/SIZE SELECT STORE    UPC    PRODUCTION CODE    USE BY OR BEFORE    POSSIBLE DISTRIBUTION STATES IN SELECT STORES
Fresh Express America's Fresh Old Fashioned Cole Slaw™
14 oz      071279123011      Z178 or Lower      Jul-13    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express America's Fresh 3 Color Deli Cole Slaw™ 14 oz      071279123004      Z178 or Lower      Jul-14    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Chopped Kit Asian 12 oz      071279302027      Z178 or Lower      Jul-13    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Chopped Kit Bacon & Bleu 10.9 oz      071279306063      Z178 or Lower      Jul-12    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Chopped Kit BBQ Ranch 11.3 oz      071279309071      Z178 or Lower      Jul-12    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Chopped Kit Chipotle Cheddar 11.4 oz      071279306049      Z178 or Lower      Jul-12    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Chopped Kit Pomegranate 10.3 oz      071279309101      Z178 or Lower      Jul-14    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Chopped Kit Poppyseed 11.7 oz      071279309118      Z178 or Lower      Jul-14    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Chopped Kit Southwest 5 oz      071279306025      Z178 or Lower      Jul-12    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Chopped Kit Sunflower Crisp 11.1 oz      071279309064      Z178 or Lower      Jul-13    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Chopped Kit Thai 'N' Cashews 11.7 oz      071279309248      Z178 or Lower      Jul-11    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Chopped Kit Thai 'N' Cashews 11.7 oz    071279309248    Z178 or Lower    Jul-12    AR, IA, IN, IL, MN, MO, SD, WI
Fresh Express Fancy Greens 7 oz      071279241005      Z178 or Lower      Jul-11    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Farmer's Garden 9 oz      071279281025      Z178 or Lower      Jul-9    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Gourmet Cafe Creative Classics Chopped Asian 6.25 oz      071279407111      Z178 or Lower      Jul-9    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Gourmet Cafe Creative Classics Mediterranean 12 oz      071279407142      Z178 or Lower      Jul-9    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Gourmet Cafe Creative Classics Turkey & Bacon Chef 5.75 oz      071279407081      Z178 or Lower      Jul-11    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Green & Crisp / Verde y Crujiente 11 oz      071279108049      Z178 or Lower      Jul-11    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Green & Crisp / Verde y Crujiente 11 oz      071279108049      Z178 or Lower      Jul-7    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Iceberg Garden / Lechuga Repollo 12 oz      071279103020      Z178 or Lower      Jul-10    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Iceberg Garden / Lechuga Repollo 24 oz      071279104119      Z178 or Lower      Jul-12    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Iceberg Garden / Lechuga Repollo 3 lbs.      071279106014      Z178 or Lower      Jul-11    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Iceberg Garden / Lechuga Repollo 12 oz      071279103020      Z178 or Lower      Jul-11    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Italian 9 oz      071279211008      Z178 or Lower      Jul-11    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Lettuce Trio / Lechuga Trío 9 oz      071279108094      Z178 or Lower      Jul-11    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Premium Romaine / Lechuga Romana Especial 9 oz      071279108087      Z178 or Lower      Jul-11    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Premium Romaine / Lechuga Romana Especial 9 oz      071279108087      Z178 or Lower      Jul-11    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Premium Slaw Salad Kit Asian Avocado 9.7 oz      071279126043      Z178 or Lower      Jul-10    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Premium Slaw Salad Kit Smoked BBQ Sriracha 11.1 oz      071279126029      Z178 or Lower      Jul-10    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express SHREDS Iceberg 14 oz      071279152004      Z178 or Lower      Jul-11    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express SHREDS 8 oz      071279151014      Z178 or Lower      Jul-10    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Veggie Lover's 11 oz      071279281001      Z178 or Lower      Jul-9    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Fresh Express Veggie Spring Mix 7 oz      071279281049      Z178 or Lower      Jun-25    AR, CT, DC, DE, IA, IL, IN, KS, KY, MA, MD,
ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ,
NY, OH, OK, PA, RI, SD, TN, VA, VT, WI, WV
Giant Eagle American (Family
Size) 24 oz    030034930370    Z178 or Lower    Jul-9    MD, OH, PA, WV
Giant Eagle Chopped Asian
Style Salad Kit 12 oz    030034923310    Z178 or Lower    Jul-11    MD, OH, PA, WV
Giant Eagle Chopped BBQ
Ranch Salad Kit 11.3 oz    030034923303    Z178 or Lower    Jul-12    MD, OH, PA, WV
Giant Eagle Chopped Chipotle
Cheddar Salad Kit 11.4 oz    030034923389    Z178 or Lower    Jul-11    MD, OH, PA, WV
Giant Eagle Chopped
Mediterranean Salad Kit 9.9 oz    030034923372    Z178 or Lower    Jul-9    MD, OH, PA, WV
Giant Eagle Chopped Southwest Style Salad Kit
11.5 oz      030034923327      Z178 or Lower      Jul-11      MD, OH, PA, WV
Giant Eagle Chopped Sunflower
Crisp Salad Kit 11.1 oz    030034923396    Z178 or Lower    Jul-10    MD, OH, PA, WV
Giant Eagle Life’s Getting
Fresher Coleslaw 16 oz    030034923099    Z178 or Lower    Jul-12    MD, OH, PA, WV
Giant Eagle Life’s Getting Fresher Fresh American Blend
11 oz      030034923105      Z178 or Lower      Jul-11      MD, OH, PA, WV
Giant Eagle Life’s Getting
Fresher Fresh Garden Salad Blend 12 oz      030034923198      Z178 or Lower      Jul-11      MD, OH, PA, WV
Giant Eagle Life’s Getting
Fresher Fresh Italian Blend 9 oz    030034923112    Z178 or Lower    Jul-11    MD, OH, PA, WV
Giant Eagle Life’s Getting
Fresher Fresh Romaine Garden Salad Blend 12 oz      030034923167      Z178 or Lower      Jul-11      MD, OH, PA, WV
Giant Eagle Life’s getting
Fresher Fresh Shredded Iceberg Lettuce 8 oz      030034923150      Z178 or Lower      Jul-10      MD, OH, PA, WV
Giant Eagle Life’s Getting
Fresher Veggie Lovers 11 oz    030034923280    Z178 or Lower    Jul-9    MD, OH, PA, WV
Giant Eagle Shredded Lettuce
16 oz    030034923204    Z178 or Lower    Jul-10    MD, OH, PA, WV
Hy-Vee American Salad Mix
12 oz    075450120479    Z178 or Lower    Jul-12    IA, IL, KS, MN, MO, NE, SD, WI
Hy-Vee Chopped Kit Asian
Salad 13.7 oz    075450246681    Z178 or Lower    Jul-11    IA, IL, KS, MN, MO, NE, SD, WI
Hy-Vee Chopped Kit Avocado
Ranch Salad 12.8 oz    075450247152    Z178 or Lower    Jul-8    IA, IL, KS, MN, MO, NE, SD, WI
Hy-Vee Chopped Kit Chipotle
Cheddar Salad 11.4 oz    075450246728    Z178 or Lower    Jul-8    IA, IL, KS, MN, MO, NE, SD, WI
Hy-Vee Chopped Kit Southwest
Salad 13.4 oz    075450246698    Z178 or Lower    Jul-11    IA, IL, KS, MN, MO, NE, SD, WI
Hy-Vee Chopped Kit Sunflower
Crunch Salad 13.2 oz    075450246704    Z178 or Lower    Jul-11    IA, IL, KS, MN, MO, NE, SD, WI
Hy-Vee Cole Slaw Mix 16 oz    075450120516    Z178 or Lower    Jul-9    IA, IL, KS, MN, MO, NE, SD, WI
Hy-Vee Garden Salad 12 oz    075450246742    Z178 or Lower    Jul-3    IA, IL, KS, MN, MO, NE, SD, WI
Hy-Vee Greener Supreme Salad
Mix 12 oz    075450120462    Z178 or Lower    Jul-11    IA, IL, KS, MN, MO, NE, SD, WI
Hy-Vee Italian Salad Mix 10 oz    075450120486    Z178 or Lower    Jul-11    IA, IL, KS, MN, MO, NE, SD, WI
Hy-Vee Romaine Salad Mix
12 oz    075450120585    Z178 or Lower    Jul-11    IA, IL, KS, MN, MO, NE, SD, WI
Hy-Vee Shredded Lettuce 8 oz    075450120530    Z178 or Lower    Jul-6    IA, IL, KS, MN, MO, NE, SD, WI
Hy-Vee Veggie Deluxe Salad
Mix 12 oz    075450085303    Z178 or Lower    Jul-10    IA, IL, KS, MN, MO, NE, SD, WI
Little Salad Bar Asian Chopped
Salad Kit 12 oz    4099100086966    Z178 or Lower    Jul-9    AR, IA, IN, IL, MN, MO, SD, WI
Little Salad Bar Chef Salad
6.2 oz    4099100107364    Z178 or Lower    Jul-9    AR, IA, IN, IL, MN, MO, SD, WI
Little Salad Bar Classic
Coleslaw 14 oz    0041498302177    Z178 or Lower    Jul-11    AR, IA, IN, IL, MN, MO, SD, WI
Little Salad Bar Garden Salad
12 oz    4099100082975    Z178 or Lower    Jul-3    AR, IA, IN, IL, MN, MO, SD, WI
Little Salad Bar Southwest
Chopped Salad Kit 12 oz    4099100087024    Z178 or Lower    Jul-8    AR, IA, IN, IL, MN, MO, SD, WI
Little Salad Bar Sunflower
Chopped Salad Kit 11.1 oz    04099100087901    Z178 or Lower    Jul-12    AR, IA, IN, IL, MN, MO, SD, WI
Marketside Baby Greens Salad
6 oz    681131027922    Z178 or Lower    Jul-7    IA, MI, MN, ND, NE, SD, WI
Marketside Chopped Salad Kit
Asian 13.7 oz    681131007047    Z178 or Lower    Jul-7    IA, MI, MN, ND, NE, SD, WI
Marketside Chopped Salad Kit
Avocado Ranch 9.5 oz    681131221320    Z178 or Lower    Jul-8    IA, MI, MN, ND, NE, SD, WI
Marketside Chopped Salad Kit Cherry Almond Gorgonzola
3.8 oz      681131148375      Z178 or Lower      Jul-6      IA, MI, MN, ND, NE, SD, WI
Marketside Chopped Salad Kit
Kale Pecan Cranberry    681131221528    Z178 or Lower    Jul-8    IA, MI, MN, ND, NE, SD, WI
Marketside Chopped Salad Kit
Southwest 13.4 oz    681131007061    Z178 or Lower    Jul-10    IA, MI, MN, ND, NE, SD, WI
Marketside Chopped Salad Kit Sunflower Bacon Crunch
13.8 oz      681131148344      Z178 or Lower      Jul-8      IA, MI, MN, ND, NE, SD, WI
Marketside Chopped Salad Kit Sunflower Bacon Crunch
22.1 oz      681131276535      Z178 or Lower      Jul-8      IA, MI, MN, ND, NE, SD, WI
Marketside Classic Iceberg
Salad 12 oz    681131328944    Z178 or Lower    Jul-7    IA, MI, MN, ND, NE, SD, WI
Marketside Classic Iceberg
Salad 24 oz    681131328951    Z178 or Lower    Jul-7    IA, MI, MN, ND, NE, SD, WI
Marketside Crisp Greens
12 oz    681131387552    Z178 or Lower    Jul-7    IA, MI, MN, ND, NE, SD, WI
Marketside Kale Slaw 12 oz    681131221573    Z178 or Lower    Jul-6    IA, MI, MN, ND, NE, SD, WI
Marketside Premium Romaine
Salad 18 oz    681131388078    Z178 or Lower    Jul-8    IA, MI, MN, ND, NE, SD, WI
Marketside Premium Romaine
Salad 9 oz    681131387538    Z178 or Lower    Jul-10    IA, MI, MN, ND, NE, SD, WI
Marketside Shredded Iceberg
Lettuce 16 oz    681131532099    Z178 or Lower    Jul-10    IA, MI, MN, ND, NE, SD, WI
Marketside Shredded Iceberg
Lettuce 8 oz    681131328968    Z178 or Lower    Jul-9    IA, MI, MN, ND, NE, SD, WI
Marketside Tri-Color Cole Slaw
14 oz    681131387484    Z178 or Lower    Jul-10    IA, MI, MN, ND, NE, SD, WI
Signature Farms Coleslaw
3 Color 14 oz    021130111961    Z178 or Lower    Jul-13    IA, IN, IL
Signature Farms Garden Salad
12 oz    021130981359    Z178 or Lower    Jun-27    IA, IN, IL
Signature Farms Lettuce Shreds
8 oz    021130112180    Z178 or Lower    Jul-3    IA, IN, IL
Signature Farms Green & Crisp
11 oz    021130419128    Z178 or Lower    Jul 14    IA, IN, IL
Signature Farms Premium
Romaine 9 oz    021130419166    Z178 or Lower    Jul 14    IA, IN, IL
Wholesome Pantry Organic Chopped Sesame Asian Salad
Kit 10.9 oz      041190066308      Z178 or Lower      Jul-12      CT, DE, MD, NJ, NY, PA
Wholesome Pantry Organic
Sesame Asian Salad Kit 13 oz    041190066292    Z178 or Lower    Jul-11    CT, DE, MD, NJ, NY, PA

Jewel-Osco Voluntarily Recalls Bagged Signature Farms Garden Salad Due to Possible Cyclospora Contamination

June 25, 2020

More Information

In cooperation with the Fresh Express recall of bagged salads potentially linked to an outbreak of Cyclospora infections in the Midwest, Jewel-Osco is voluntarily recalling bagged Signature Farms Garden Salad sold in its stores in Illinois, Indiana, and Iowa.
The recalled Signature Farms Garden Salad was sold in 12-ounce bags in the Produce section. The recalled products have BEST IF USED BY dates of May 16 through July 4 (5-16-20 through 7-04-20). The BEST IF USED BY date is printed on the top right corner of the front of the package. The product has a UPC code of 21130 98135, which can be found on the back of the package and bears the unique plant number S5417.
Cyclospora cayetanensis is a microscopic parasite of humans. This parasite, when it contaminates food or water and is then ingested, can cause an intestinal illness called cyclosporiasis. Most people infected with Cyclospora develop diarrhea. Other common symptoms include loss of appetite, weight loss, stomach cramps/pain, bloating, increased gas, nausea, and fatigue. Vomiting, body aches, headache, fever, and other flu-like symptoms may be noted. Some people who are infected with Cyclospora do not have any symptoms. If not treated, the illness may last from a few days to a month or longer. Symptoms may seem to go away and then return one or more times.
Consumers are asked to check their refrigerators for the recalled product. Consumers who have purchased the product are asked to discard or return it to the place of purchase for a refund. Customers who have questions about the recall can contact Jewel-Osco at 1-877-723-3929.

Pilgrim's Pride Corporation Recalls Chicken Breast Nugget Products due to Possible Foreign Matter Contamination

June 28, 2020

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Pilgrim’s Pride Corporation, a Waco, Texas establishment, is recalling approximately 59,800 pounds of fully cooked chicken breast nugget products that may be contaminated with extraneous materials, specifically flexible rubber material, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The frozen ready-to-eat (RTE) chicken breast nugget items were produced on May 6, 2020. The following products are subject to recall [View Labels (PDF Only)] : 
•    4-lb. plastic bag packages containing “Pilgrim’s FULLY COOKED CHICKEN BREAST NUGGETS,” with a Best-By date of 06 MAY 2021 and lot code of 0127 printed on the retail package. Product cases contain lot codes 0127105009, 0127105010, 0127105011, 0127105012, 0127105013, 0127105014, 0127105015, or 0127105016 printed on the box.
The products subject to recall bear establishment number “P-20728” printed on individual retail packages as well as product cases. These items were shipped to retail locations in Arizona, Idaho, Oregon, and Texas.                       
The problem was discovered after the firm received a consumer complaint reporting rubber pieces in the chicken breast nuggets product.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
Consumers with questions about the recall can contact Ed Tyrrell, Consumer Relations Manager for Pilgrim’s Pride Corporation, at (800) 321-1470. Members of the media with questions about the recall can contact Nikki Richardson, Director of Communications for Pilgrim’s Pride Corporation, at (970) 506-8028.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.
https://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2020/recall-014-2020-release

Fresh Express Announces Precautionary Recall of a Limited Quantity of Southwest Chopped Kit Due to the Presence of Undeclared Allergens

June 22, 2020

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Fresh Express is voluntarily recalling a limited quantity of Fresh Express 11.5-ounce Southwest Chopped Kit with production codes G163B10A and G163B10B, UPC code 0 71279 30602 5 and use-by date of June 29 due to the presence of undeclared wheat, soy, cashews, and coconut. In some individuals the consumption of undisclosed allergens could cause allergic reactions that in some cases could be life-threatening.
The recall was necessitated when Fresh Express learned that, during a single production run, incorrect condiment packets were placed into Southwest Chopped Kit bags and, as a result, the allergens wheat, soy, cashews, and coconut are not properly declared.
Only the Southwest Chopped Kit displaying the identified product codes, UPC code and use-by date are subject to the recall. All other Fresh Express Southwest Chopped Kits are properly labeled, and no other Fresh Express products are included in the recall. No illnesses are reported to date.
The recalled product was distributed between June 12 and June 18 in the states of Alabama, Delaware, Florida, Georgia, Kentucky, Maryland, North Carolina, South Carolina, Tennessee, Virginia, and West Virginia. Fresh Express representatives are coordinating with retail stores, instructing them to remove the recalled product from store shelves and inventories.
Fresh Express takes all matters of food safety very seriously, including the issue of allergens. Company procedures and programs stringently follow all mandated regulations and focus on preventive measures designed to minimize potential risks. Express is coordinating with the U.S. Food and Drug Administration and is conducting a full investigation into this isolated incident.
Consumers in possession of the recalled product should discard it. A refund is available where purchased or by contacting the Fresh Express Consumer Response Center toll-free at (800) 242-5472 Monday through Friday during the hours of 7 a.m. to 5 p.m. Eastern time.
Recalled Product Details
•    Fresh Express Southwest Chopped Kit - 11.5-oz. bag
•    Product Codes G163B10A and G163B10B with use-by date of June 29, located in the upper righthand corner on the front of the bag
•    UPC Code of 0 71279 30602 5 located on the reverse side of the bag by the bar code
Recalled Product Distribution
Fresh Express Precautionary Recall, Southwest Chopped Kit – 06/18/2020 (No other Fresh Express salads are included in this recall)
Brand    PRODUCT NAME    SIZE    UPC    PRODUCTION CODE    BEST IF
USED BY DATE    POSSIBLE
DISTRIBUTION STATES
Fresh Express    Southwest Chopped Kit    11.5-oz.    071279 306025    G163B10A
G163B10B    Jun-29    AL, DE, FL, GA, KY,
MD, NC, SC, TN, VA, WV

La Bodega Meat LLC Recalls Beef Products Distributed Without Benefit of Import Re-Inspection

June 17, 2020

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WASHINGTON, June 17, 2020 - La Bodega Meat LLC, a Farmers Branch, Texas establishment, is recalling approximately 83,038 pounds of raw beef products that were not presented for import re-inspection into the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The various raw beef items were imported on June 2 and June 3, 2020. The following products are subject to recall: [View Label (PDF Only)] 
•    51.90-lb. boxes containing various cuts of beef, including: 
o    “BONELESS RIBEYE ROLL”
o    “FLANK STEAK”
o    “FRESH BONELESS BRISKET”
o    “FRESH EYE OF ROUND”
o    “FRESH FLAP MEAT”
o    “FRESH INSIDE SKIRT”
o    “FRESH OUTSIDE ROUND”
o    “FRESH TOP SIRLOIN”
o    “INSIDE ROUND”
o    “OUTSIDE SKIRT”
o    “PEELED KNUCKLE”
o    “SHOULDER CLOD”
The products subject to recall bear establishment number “ESTABLISHMENT 5” inside the foreign mark of inspection. The boxes also contain shipping marks 0671-20 or 0627-20. These items were shipped to distributor locations in Arkansas, Missouri, and Texas for food service and retail sales. Product at the retail level will not have any unique identifying labels.           
The problem was discovered during routine FSIS surveillance activities of imported products.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.  
FSIS is concerned that some product may be in distributors’, retailers’ and consumers’ refrigerators or freezers. Distributors in possession of these products are urged not to further distribute them. Retailers who have obtained these products are urged not to sell them. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers and members of the media with questions about the recall can contact Jose Torres, Director, La Bodega Meat LLC at (214) 402-4966.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/. 

Rusty’s Seafood Market Issues Allergy Alert on Undeclared Allergens (Fish, Crustacean, Shellfish, Eggs, Milk, Soy, and Wheat) in all “Captain Rusty’s Seafood Dips”

June 16, 2020

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Rusty’s Seafood Market of Lorida, Florida, is recalling all five of its Captain Rusty’s Seafood Dips due to the presence of undeclared allergens. People who have allergies to fish (mahi, salmon, whiting, pollock, threadfin bream), crustacean shellfish (crab, lobster, shrimp), wheat, eggs, soy or milk run the risk of serious or life-threatening allergic reaction if they consume these products.
The recalled Captain Rusty’s Seafood Dips were distributed in South Florida, Sarasota, FL., Tampa, FL. and Lorida, FL. through distributors and retail markets. The product comes in a 7-ounce, clear plastic container, 16-ounce clear plastic container and 6 lb white plastic buckets. The lot code is located on the bottom of the container and the expiration date is located on the top label.
The following products with lot codes (in bold) and expiration dates are being recalled:
Captain Rusty’s Smoked Salmon Dip 2015-6/16/20, 2023-6/23/20.
Captain Rusty’s Smoked Mahi Dip 1999-6/1/20, 2002-6/6/20, 2009-6/13/20, 2010-6/14/20, 2011-6/16/20, 2017-6/17/20, 2019-6/21/20
Captain Rusty’s Lobster Dip 1992-5/30/20, 1998-6/1/20, 2000-6/6/20, 2005-6/7/20, 2014-6/16/20
Captain Rusty’s Cajun Crab and Lobster Dip 1994-5/30/20, 1996-6/1/20, 2004-6/7/20, 2006-6/11/20, 2008-6/11/20, 2013-6/16/20, 2018-6/17/20, 2021-6/23/20
Captain Rusty’s Blue Crab Dip 1993-5/30/20, 1997-6/1/20, 2001-6/6/20, 2003-6/7/20, 2007-6/11/20, 2012-6/16/20, 2020-6/21/20, 2022-6/23/20
There have been no confirmed illnesses reported to date.
The recall was initiated after the Florida Department of Agriculture and Consumer Services (FDACS) determined, during routine inspection, that the product containing allergens was distributed in packaging that did not identify the presence of fish (mahi, salmon, whiting, pollock, threadfin bream), crustacean shellfish (crab, lobster, shrimp), wheat, eggs, soy or milk. Subsequent investigation indicates the problem was caused by a breakdown in the company’s labeling process.
Customers can return any product for a complete refund, please contact Captain Rusty Seafood @ 813-244-2799, Monday through Friday from 12:00PM - 6:00PM EST.

NOW Health Group Inc. Voluntarily Recalls NOW Real Food ®Raw Macadamia Nuts Because of Possible Health Risk

June 16, 2020

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NOW Health Group, Inc. (NOW), of Bloomingdale, Illinois, is voluntarily recalling its NOW Real Food® Raw Macadamia Nuts – Product Code 7119, Lot#3141055 – because this lot has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis, and arthritis.
This lot was distributed online and in retail stores nationwide.
Recalled products include:
Item Number    Description    Lot Number    Best By Date
7119    NOW Real Food® Raw Macadamia Nuts, Unsalted, 8 oz. pouch    3141055    01/2021
No other NOW Real Food® products are affected or are involved in this recall. No illnesses have been reported to date in connection with this product.
NOW became aware of the potential contamination after routine sampling in a later lot of finished product (which contained the same lot of raw material as used in the recalled lot) found the bacteria. This later finished product lot was not released and remains in a quarantined state.
NOW has provided information on this recall to all its retailers who purchased this product and has encouraged retailers to make every effort to contact their customers to facilitate the return of affected products.
Consumers who have purchased the recalled Raw Macadamia Nuts should stop using the product immediately and return it to place of purchase for a full refund. Receipt is not required for refund.
Consumers with questions regarding this recall can contact NOW’s Customer Service Department by phone at 888-NOW-FOOD (888-669-3663) Monday through Friday, 8:00 a.m. to 5:00 p.m. Central time.

Lakeside Refrigerated Services Recalls Beef Products due to Possible E.coli O157:H7 Contamination

June 13, 2020

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WASHINGTON, June 13, 2020 – Lakeside Refrigerated Services, a Swedesboro, N.J. establishment, is recalling approximately 42,922 pounds of ground beef products that may be contaminated with E. coli O157:H7, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The raw ground beef items were produced on June 1, 2020. The following products are subject to recall: [View Labels (PDF Only)]  
•    1-lb. vacuum packages containing “MARKETSIDE BUTCHER ORGANIC GRASS-FED GROUND BEEF” and a use or freeze by date of 07/01/20 and lot code P-53298-82.
•    1-lb. vacuum packages containing four ¼ lb. pieces of “MARKETSIDE BUTCHER ORGANIC GRASS-FED GROUND BEEF PATTIES” and a use or freeze by date of June 27, 2020 and lot code P-53934-28.
•    3-lb. vacuum packages containing three 1 lb. pieces of “MARKETSIDE BUTCHER ORGANIC GRASS-FED GROUND BEEF 93% LEAN / 7% FAT” and a use or freeze by date of 07/01/20 and lot code P53929-70.
•    1-lb. tray packages containing four ¼ lb. pieces of “THOMAS FARMS GRASS-FED GROUND BEEF PATTIES 85% LEAN / 15% FAT” and a use or freeze by date of 06/25/20 and lot code P53944-10.
•    4-lb. tray packages containing 10 ¼ lb. pieces of “THOMAS FARMS GRASS-FED GROUND BEEF PATTIES 80% LEAN / 20% FAT” and a use or freeze by date of 06/25/20 and lot code P53937-45.
•    1-lb. vacuum packages containing four ¼ lb. pieces of “THOMAS FARMS GRASS-FED GROUND BEEF PATTIES 85% LEAN / 15% FAT” and a use or freeze by date of 06/27/20 and lot code P53935-25.
•    1-lb. vacuum packages containing “VALUE PACK FRESH GROUND BEEF 76% LEAN / 24% FAT” and a use or freeze by date of 07/01/20 and lot code P53930-18.
The products subject to recall bear establishment number “EST. 46841” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.
The problem was discovered during routine FSIS testing. There have been no confirmed reports of adverse reactions due to consumption of these products.
Anyone concerned about an injury or illness should contact a healthcare provider. E. coli O157:H7 is a potentially deadly bacterium that can cause dehydration, bloody diarrhea and abdominal cramps 2–8 days (3–4 days, on average) after exposure the organism. While most people recover within a week, some develop a type of kidney failure called hemolytic uremic syndrome (HUS). This condition can occur among persons of any age but is most common in children under 5-years old and older adults. It is marked by easy bruising, pallor, and decreased urine output. Persons who experience these symptoms should seek emergency medical care immediately.
FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
FSIS advises all consumers to safely prepare their raw meat products, including fresh and frozen, and only consume ground beef that has been cooked to a temperature of 160°F. The only way to confirm that ground beef is cooked to a temperature high enough to kill harmful bacteria is to use a food thermometer that measures internal temperature, https://www.fsis.usda.gov/safetempchart.
Consumers and members of the media with questions about the recall can contact the Lakeside Processing Center Call Center at (856) 832-3881.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.
https://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2020/recall-012-2020-release

Nestle Prepared Foods Company Recalls Lean Cuisine Fettuccini Alfredo Products Due to Misbranding and Undeclared Allergens

May 29, 2020

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WASHINGTON, May 28, 2020 – Nestle Prepared Foods Company, a Jonesboro, Ark. establishment, is recalling approximately 29,002 pounds of chicken product labeled as Lean Cuisine Fettuccini Alfredo because the product contains undeclared soy, a known allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The Lean Cuisine Fettuccini Alfredo is not supposed to contain chicken and chicken does not appear in the ingredients statement or on the label.[View Labels (PDF Only)]  
The frozen, Lean Cuisine Fettuccini Alfredo products were produced and packaged on April 22, 2020. The following products are subject to recall:
•    9 1/4-oz. retail carton containing “LEAN CUISINE favorites Fettuccini Alfredo tender pasta with a creamy cheese sauce” with a lot code “0113587812 A,” “0113587812 B,” “0113587812 C,” or “0113587812 D” and a date of “MAY 2021” on side of the label.
The products subject to recall bear establishment number “P27333” printed on the package next to the lot code. The products were distributed in shipping cartons labeled as LC Chicken Fettuccini bearing the mark of inspection. These items were shipped to retail locations nationwide.
The problem was discovered when the firm received multiple consumer complaints that the product labeled as Lean Cuisine Fettuccini Alfredo contained chicken that is not referenced on the label or ingredients.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers.
Consumers with questions about the recall can contact Nestle Prepared Foods Company here or (800) 993-8625. Members of the media with questions about the recall can contact Kate Shaw, Nestlé USA Corporate Communications, at kate.shaw@us.nestle.com.  
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Conagra Brands, Inc. Recalls Frozen Not-Ready-To-Eat Chicken and Turkey Bowl Products due to Possible Foreign Matter Contamination

May 22, 2020

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WASHINGTON, May 22, 2020 – Conagra Brands, Inc., Russellville, Ark. and Marshall, Mo. establishments, are recalling approximately 276,872 pounds of not ready-to-eat chicken and turkey bowl products because the products may contain extraneous material, specifically small rocks, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The scope of this recall has been expanded to include Healthy Choice Power Bowls Chicken Feta & Farro Bowls, Healthy Choice Power Bowls Unwrapped Burrito Scramble Power Bowls, and Healthy Choice Power Bowls Turkey Sausage & Egg Scramble Power Bowls produced on various dates. The products were produced at two different establishments.
The following additional products are subject to recall: [View Labels (PDF Only)]
•    9.5-oz cartons containing “Healthy Choice POWER BOWLS Chicken Feta & Farro” with lot code 5006006620 and best by date of DEC 01 2020. The product bears establishment number “P-115” on the side panel adjacent to the lot code.
•    7.2-oz cartons containing “Heathy Choice POWER BOWLS Unwrapped Burrito Scramble” with UPC 7265500082, lot code 5009002920 and best if used by date of OCT 25 2020. The product bears establishment number “P9” on the side panel adjacent to the lot code.
•    7.2-oz cartons containing “Healthy Choice POWER BOWLS Turkey Sausage & Egg White Scramble” with UPC 7265500081, lot code of 5009003020 and a best if used by date of OCT 26 2020 on the label. The product bears establishment number “P9” on the side panel adjacent to the lot code.
•    204-gram cartons containing “Healthy Choice POWER BOWLS BOILS ÈNERGIE PETIT DÈJJEUNER TOUTE JOURNÈE Turkey Sausage & Egg White Scramble” with UPC 7265500202, lot code of 5009003020 and a best if used by date of OCT 26 2020 on the label. The product bears establishment number “EST P9” on the side panel adjacent to the lot code.
•    204-gram cartons containing “Heathy Choice POWER BOWLS BOILS ÈNERGIE PETIT DÈJJEUNER TOUTE JOURNÈE Unwrapped Burrito Scramble” with UPC 7265500203, lot code 5009002920 and best if used by date of OCT 25 2020. The product bears establishment number “EST P9” on the side panel adjacent to the lot code.
On April 10, 2020. Conagra Brands, Inc., recalled approximately 130,763 pounds of not ready-to-eat chicken bowl products produced on Jan. 23, 2020. The products bear establishment number “EST P115” inside the USDA Mark of inspection.
•    9.5-oz. cartons containing “Healthy Choice POWER BOWLS Chicken Feta & Farro” with lot code 5006002320, UPC code 072655001800 and a best by date of 10/19/2020 on the label.
•    9.5-oz. cartons containing “Healthy Choice POWER BOWLS Chicken Feta & Farro, BOILS ÈNERGIE Poulet feta et épeautre” with lot code 5006002320, UPC code 072655003026 and a best by date of 10/19/2020 on the label.
These items were shipped to retail locations nationwide and exported to Canada.            
The problem was discovered when the firm received additional consumer complaints about rocks being in the products and the firm then notified FSIS of the issue.
 There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.  
FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers with questions about the recall can contact Conagra Brands Consumer Care at 1-800-672-8240 or at Consumer.Care@conagra.com. Members of the media with questions about the recall can contact Daniel Hare, Conagra Brands Senior Director of Communication, at (312) 549-5355.
Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 1-888-MPHotline (1-888-674-6854) or live chat via Ask USDA from 10 a.m. to 6 p.m. (Eastern Time) Monday through Friday. Consumers can also browse food safety messages at Ask USDA or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.
https://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2020/recall-007-2020-exp-release

New Hoque and Sons, Inc. Recalls Radhuni Curry Powder Because of Possible Health Risk

May 21, 2020

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New Hoque and Sons, Inc. of Maspeth, NY is recalling Radhuni Curry Powder, contained in 400g plastic bottles, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
Radhuni Curry Powder was distributed in New York City, New York, including grocery stores in Jamaica, Jackson Heights, and the Bronx. The product was distributed to grocery stores between 4/17/2020 and 4/21/2020. They were then physically removed from the stores on 5/14/2020.
The product is labeled “Radhuni Curry Powder”. The product is contained in 400g clear, plastic bottles, with an expiration date of 01/02/2022, which can be found printed on the side of the container.
No illnesses have been reported to date.
The recall was as the result of a routine sampling program by the FDA, which revealed that the finished products contained the bacteria. The company has ceased the distribution of the contaminated products and has also physically removed the contaminated products from stores as FDA and New Hoque and Sons, Inc. continue their investigation as to what caused the problem.
Consumers who have purchased Radhuni Curry Powder are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 718.391.0992 from Monday - Friday between the hours of 9am and 5pm EST.

Ramar Foods Recalls Mint Chocolate Chip With Hidden Spinach Ice Cream Because of Possible Health Risk

May 14, 2020

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Ramar Foods of Pittsburg, CA, is recalling its 14 ounce packages of Peekaboo branded Mint Chocolate Chip with Hidden Spinach Ice Cream product out of an abundance of caution because of the potential contamination of Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The ice cream product being recalled was available for purchase at select Target stores in FL, GA, SC, and NC. Only thirty-three (33) containers of the ice cream product were purchased by consumers and the remaining containers have been removed from commerce. The ice cream affected comes in a 14 ounce, printed paper container with UPC# 8685400001, and a Best Before date of 10/08/2021 printed on the bottom.
No illnesses have been reported to date in connection with this product.
The potential for contamination was discovered after internal routine testing by Ramar Foods revealed the presence of Listeria monocytogenes in some packages of the ice cream.
Production of the recalled product has been voluntarily suspended while we continue to work with FDA to investigate and take appropriate corrective measures.
Consumers who purchased the Peekaboo branded Mint Chocolate Chip with Hidden Spinach with the
Best Buy date of 10/08/2021 should not consume the product and will be offered a full refund.
Consumers with questions, or who would like to request an immediate refund, may contact Ramar Foods. Consumer contact: 844-491-7869, M-F 8-5pm EST; ramarfoods5691@stericycle.com.

Mellace Family Brands California Inc. (Johnvince Foods) Recalls Wegmans Semi-Sweet Chocolate nonpareils, 18.5oz (1lb 2.5oz) 524g Due to Undeclared Milk Allergen

May 14, 2020

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MELLACE FAMILY BRANDS CALIFORNIA INC. (JOHNVINCE FOODS),located at 655 North River Road, Unit C, Warren Ohio 44483-2254, is recalling Wegmans Semi-Sweet Chocolate nonpareils, 18.5oz (1lb 2.5oz) 524g because it has undeclared MILK allergen on the retail label. People who have an allergy or severe sensitivity to MILK run the risk of a serious or life-threatening allergic reaction if they consume this product.
This product was distributed within Maryland, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania and Virginia. Product was sold to consumers through Wegmans retail stores.
The retail unit is a plastic tub with a tamper evident seal and pre-printed label. Brand “WEGMANS”, product description WEGMANS SEMI-SWEET CHOCOLATE NONPAREILS, 18.5OZ (1LB 2.5OZ) 524g UPC: 77890-49787. Best by dates: 12/18/20 and 12/28/20
No illnesses have been reported to date.
The recall was initiated after it was discovered that the above product containing Milk was distributed in packaging that did not reveal the presence of Milk.
REFUND INFORMATION:
Customers may return product to the Wegmans Service Desk for a full refund.
FOR MORE INFORMATION, CONTACT:
Wegmans Food Markets at 1-855-934-3663 Monday through Friday from 8:00 AM - 6:00 PM EST or Saturday and Sunday from 8:00 AM - 5:00 PM EST.

UNFI Voluntarily Recalls Wild Harvest® Organic Basil Due to Possible Health Risk

May 11, 2020

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United Natural Foods, Inc. (UNFI) is initiating a voluntary recall of a limited quantity of Wild Harvest® Organic Basil distributed out of UNFI’s Hopkins, MN distribution center to select retailers in Minnesota between 4/18/2020-5/8/2020. UNFI’s recall is issued out of an abundance of caution because of the potential for the impacted product to be contaminated by Cyclospora cayetanensis. No illnesses, including allergic reactions, involving this product have been reported to date.
This recall includes Wild Harvest® Organic Fresh Basil products sold in .25oz, .75oz, 2oz, and 4oz plastic clam shell containers (UPCs: 0071153550450, 0071153550322, 0071153550762, 0071153550323). Impacted product can be identified by a white sticker with black ink on the back of the container stating: “Product of Colombia” and “112.”
This concern was identified following routine sampling. Cyclospora cayetanensis is a microscopic parasite that can cause an intestinal illness in people called cyclosporiasis. According to the U.S. Centers for Disease Control and Prevention, the illness is usually not life threatening. Symptoms of cyclosporiasis may include: watery diarrhea (most common), loss of appetite, weight loss, cramping, bloating, increased gas, nausea and fatigue. Other symptoms that may occur but are less common include vomiting and low-grade fever.
This recall is being initiated with the knowledge of the United States Food & Drug Administration. This product was distributed in the state of Minnesota to grocery stores. Consumers who believe that they are in possession of any of the above products affected by this recall should dispose of the product in an appropriate waste container. For any inquiries, consumers may call 1-888-256-2800.
About United Natural Foods
UNFI is North America's premier food wholesaler delivering the widest variety of products to customer locations throughout North America including natural product superstores, independent retailers, conventional supermarket chains, ecommerce retailers, and food service customers. By providing this deeper 'full-store' selection and compelling brands for every aisle, UNFI is uniquely positioned to deliver great food, more choices, and fresh thinking to customers everywhere. Today, UNFI is the largest publicly-traded grocery distributor in America. To learn more about how UNFI is Moving Food Forward, visit www.unfi.comExternal Link Disclaimer.

Zilk’s Plus Resources Issues Allergy Alert on Undeclared Milk, Soy, and Wheat in Select 12 Oz Bottled Sauces

May 8, 2020

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Zilk’s Plus Resources, LLC of Austin, TX announces a voluntary recall for select 12 oz bottles of Pluckers World Famous Wing Sauces because they may contain undeclared allergens. People who have an allergy or severe sensitivity to soy, milk or wheat run the risk of serious or life-threatening allergic reactions if they consume these products.
The recalled sauces were distributed to Pluckers restaurants in Texas and Louisiana on the following dates: 05/2019 – 05/2020. Consumers may have purchased such products at the affected Pluckers locations in Texas and Louisiana.
The products are packaged in a 12-ounce, clear glass bottle marked with the name of the Product Flavor (as shown below), the Pluckers brand name, and the following lot code and expiration dates located on the side, above the label. Pictures of the select product labels are attached to assist consumers with identifying the affected products.
Product Flavor    Recalled Lot Codes    Expiration Dates    Undeclared Allergen
Baker's Gold    201905063, 201909015, 201912024,
202002031A, 202003022A, 202003035A    5/21/2020, 09/09/2020, 12/16/2020,
02/03/2021, 02/09/2021, 03/04/2021    Soy and Wheat
Gochujang    201905014, 201908072, 201908137    05/24/2020, 08/19/2020, 09/03/2020    Wheat
Gold Rush    201908071, 202002131A    08/19/2020, 02/25/2021    Soy and Wheat
Hallelujah    201908030, 201909040, 201909077,
201910075    08/12/2020, 09/16/2020,
09/23/2020, 10/23/2020    Milk
Sesame    201909014    9/9/2020    Wheat
Spicy Mandarin    201904066, 201907090, 201908090,
201909073, 201910004, 202002038A,
202003156A    04/26/2020, 07/26/2020,
08/27/2020, 09/23/2020,
10/03/2020, 02/10/2021, 03/30/2021    Milk and Wheat
Teriyaki    201904081, 201905030, 201909073,
201912036, 202002033A    05/02/2020, 05/22/2020,
09/23/2020, 12/11/2020, 02/10/2021    Wheat
Vampire Killer    201909042, 202002030A, 202003015A    09/23/2020, 02/03/2021, 03/04/2021    Soy and Wheat
No illnesses have been reported to date in connection with this problem.
The recall was initiated after it was discovered that these products were distributed in packaging that did not adequately reveal the presence of soy-, wheat- or milk- containing ingredients in the affected products.
At-risk consumers who believe they may have purchased one of the affected 12-ounce bottles of Pluckers World Famous Wing Sauce flavors are urged to either dispose of the product or return it to any Pluckers location for a full refund or exchange. Consumers with questions may contact the manufacturer, Zilk’s Plus Resources, LLC, by calling 1-817-618-6298 between the hours of 10:00 am–3:00 pm CST, Monday–Friday.

The Essential Baking Company Issues Allergen Alert on Undeclared Egg in 84 Loaves of 32 Oz. Sliced Columbia Bread

May 5, 2020

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The Essential Baking Company of Seattle, Washington is recalling 84 loaves of 32 oz. Sliced Columbia Bread, expiration date May 6.20, due to undeclared egg. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume this product.
The actual product in the bags may be 16 oz. Challah Bread which was mis-labeled as Sliced Columbia Bread and the label does not declare egg. The affected product has the expiration of May 6.20 and it is found on the Kwik-Lok seal at the end of the bag.
The mislabeled Sliced Columbia was distributed in the Puget Sound Metropolitan area in Washington only on May 3, 2020. We became aware of the problem around 1pm PST on Monday, May 4, 2020 through internal review and immediately called each of the stores that received the product to have any remaining product removed from shelves.
No illnesses have been reported to date. This recall is being made with the knowledge of the U.S. Food and Drug Administration.
Consumers who have purchased this product are urged not to consume and return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1-206-545-3804 from 9am to 5pm PST.

Becca Cosmetics voluntarily recalls Light Shifter Brightening Concealer

May 7, 2020

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Out of abundance of caution, and in line with its commitment to consumer satisfaction and safety, Becca Cosmetics is voluntarily recalling all shades of its Light Shifter Brightening Concealer because a brownish-black material identified as a common household mold was found on the sponge-tip applicator of some units. While this is unlikely to cause serious injury there is a potential risk of temporary skin and/or eye allergy and irritation. To date, no adverse reactions or injuries have been reported.
This product was manufactured in the United States and distributed nationwide.
The below table provides details of the product affected by this recall. No other Becca Cosmetics products are affected by this issue.
Product Name    Batch    Size    Product Description    UPC
Becca Cosmetics
Light Shifter Brightening Concealer    0030A,
9308A,
0052A,
0052C,
9291A,
9309A,
0036A,
0037A,
0038A,
0038B,
0041A,
9289A,
0062A,
0062B,
0062C,
9283A,
9284A,
9287A,
9288A    3.2 mL (only size available)    Concealer wand with silver overlay, and a white secondary carton    9331137030037
9331137030044
9331137030051
9331137030068
9331137030075
9331137030099
9331137030082
9331137030105
If you have this product, please stop using it and contact the place of purchase regarding a refund.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Royal International Trading Inc Issues Alert On Undeclared Sulfites In “Tayni Boctoka Dry Fruits Mix Compot Apple”

April 22, 2020
 

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ROYAL INTERNATIONAL TRADING Inc of Brooklyn, NY is recalling its 500g (17.63oz) packages of "TAINY BOCTOKA DRY FRUITS MIX COMPOT APPLE" because they contain undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.
The recalled "TAINY BOCTOKA DRY FRUITS MIX COMPOST APPLE" were distributed nationwide in retail stores and through mail orders. The product comes in 500g (17.63oz) clear plastic package marked with container code 4705932006197.
No illness or allergic reactions involving this product have been reported to date.
The recall was initiated after routine sampling be New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in the500g (17.63oz) packages of "TAINY BOCTOKA DRY FRUITS MIX COMPOT APPLE" which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reaction in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individual upon ingesting 10 milligrams or more of sulfites. Analysis of the "TAINY BOCTOKA DRY FRUITS MIX COMPOT APPLE" revealed that it contained 34.4 mg per serving.
Consumers who have purchased 500g (17.63oz) packages of "TAINY BOCTOKA DRY FRUITS MIX COMPOT APPLE” are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at (347)223-1095.

Allergy Alert Issued by Buckhead Meat and Seafood of Houston, Inc. for Undeclared Wheat, Soy, Milk, Fish and Eggs in Frozen Flounder Stuffed with Seafood

April 22, 2020
 

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Buckhead Meat and Seafood of Houston, Inc., a Sysco Company, is voluntarily recalling a small quantity of frozen Flounder Stuffed with Seafood because its labeling inadvertently did not identify the following allergens in the product: wheat, soy, milk, fish, and eggs. People who have an allergy or severe sensitivity to wheat, soy, milk, fish, or eggs run the risk of a serious or life-threatening allergic reaction if they consume this product.
Flounder Stuffed with Seafood was sold to a limited number of consumers between April 1, 2020 and April 16, 2020 at various locations across the Harris County, Texas area. Nearly all customers who purchased the product have been notified directly, however the purchasers of less than 25 cases (75lbs) of the product have not been identified or notified.
The product is packaged in a brown cardboard box with the product name "FLOUNDER STUFFED W SEAFOOD FRZN." The Item Number is 7126763. The Pack Dates on the label range from 03/31/20 to 04/15/20.
Customers with allergies or sensitivities to wheat, soy, milk, fish, or eggs should discard the product or contact Buckhead Meat and Seafood of Houston to return it for a full refund.
To date, no illnesses related to this product have been reported. The issue was identified by a company employee while evaluating the product. Buckhead Meat and Seafood of Houston is working collaboratively with the U.S. Food and Drug Administration on this recall.
Buckhead Meat and Seafood of Houston takes the safety and integrity of the products it distributes seriously. Buckhead Meat and Seafood of Houston regrets any inconvenience and concern this recall may cause.
Customers who have any questions about the recall may contact Cecilia Delgado at: Cecilia.Delgado@BuckheadMeat.com or by phone at 281-405-3235 from 8:00 a.m. – 5:00 p.m. CST Monday through Friday.

Ocean Spray Cranberries, Inc Recalls Single Production Lot of 5.5 Oz Cans of Pink Lite Cranberry Juice Drink Because of Undeclared Sulfites

April 22, 2020
 

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Ocean Spray Cranberries, Inc. is recalling a single production lot of 5.5oz cans of Pink Lite Cranberry Juice Drink (listed below) because it may contain undeclared sulfites, which were erroneously added by a contract manufacturer. Sulfites are a common preservative added to many food products; however, consumers who have sensitivity to sulfites run the risk of allergic reactions if consumed. Most people will not experience any effect if they consume this ingredient. No illnesses have been reported to date.
The 5.5oz cans of Pink Lite Cranberry Juice Drink were distributed to retail supermarkets, retail wholesalers and online retailers. The single lot of product in question is sold in boxes containing six 5.5oz cans and will have any of the following code information:
•    Lot: MH0030LPK4
•    Pack Case UPC: 03120003782 4
•    Can UPC: 03120003682 7
•    GTIN Case 0003120023682 1
•    GTIN Case 0003120024682 0
•    Best Before Date: 24JAN21
•    Dates of Distribution: 21FEB2020 through 16APR20
The recall was initiated after the contract manufacturer revealed their error, subsequent to a root cause investigation of consumer complaints regarding an “off” odor in the identified lot. Analysis by the food safety and quality personnel revealed that sulfites were added to the identified lot of product erroneously by a contract manufacturer. Such sulfites are not part of the product formula and were not declared on the label. This is an isolated incident. No other Ocean Spray® products are affected by the recall. Ocean Spray is dedicated to providing safe, high-quality products.
Consumers who have purchased the 5.5 oz cans of Pink Lite Cranberry Juice Drink that contain the code information listed above are urged to please take a picture of the “best before date” code on the bottom of the can and then destroy the product. The picture should be sent to casupport@oceanspray.com. The Ocean Spray Consumer Hotline can be reached at 1-800-662-3263, weekdays 9:00 a.m. to 6:00 p.m.ET, or via the email provided 24/7, for a coupon replacement and/or for alternate methods to submitting the picture.

Allergy Alert Issued for Undeclared Cashews in Queso Sauce Sold at a Single Whole Foods Market Store in Phoenix

April 17, 2020
 

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The Whole Foods Market store located at 7111 E Mayo Blvd. Phoenix, AZ 85054 is voluntarily recalling Queso Sauce because it may contain cashews (a tree nut). People who have an allergy or severe sensitivity to tree nuts run the risk of a serious or life-threatening allergic reaction if they consume this product.
The product was available as a fresh-pack item in the prepared foods department with a sell-by date of April 14, 2020 and can be identified by the PLU code printed on the product scale labels beginning with 74135. The product labeled was sold in clear plastic deli-style containers of various weights. All affected products have been removed from store shelves. The issue was discovered after a customer reported a reaction. One reaction has been reported to date.
Customers who purchased this product at Whole Foods Market can bring a valid receipt into the store for a full refund. Consumers with additional questions can call 1-844-936-8255 between the hours of 7:00 a.m. and 10:00 p.m. CST, Monday through Friday, or 8:00 a.m. and 6:00 p.m. Saturday through Sunday.

Raw Seafoods, Inc. Issues Allergy Alert on Undeclared Wheat in Wegmans Brand Oven Safe Salmon Teriyaki and Oven Safe Ginger Salmon

March 16, 2020
 

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Raw Seafoods, Inc is initiating a limited voluntary recall of the following products:
Product Name and PLU Code    Code on Packaging    Best By Date
Wegmans Ginger Salmon, Oven Safe - 6474    7608    01/23/2021
    7659    02/13/2021
Wegmans Salmon Teriyaki, Oven Safe - 6408    7688    02/24/2021
    7692    02/25/2021
This recall is due to an undeclared wheat allergen in Wegmans branded Ginger Salmon Oven Safe Meal and Salmon Teriyaki Oven Safe Meal, which was manufactured by Raw Seafoods, Inc. for Wegmans. No illnesses or allergic reactions have been reported at this time. However, people who have an allergy to wheat may have a serious allergic reaction if they consume these products or products containing a wheat allergen.
The recalled product was distributed to Wegmans stores in New York, Massachusetts, New Jersey, Pennsylvania, Maryland, Virginia, and North Carolina.
Only Wegmans Oven Safe Meals with the specific product codes and best by dates listed above are impacted, and no other Raw Seafoods or Wegmans Brand items. The product code and best by date are listed in the bottom right corner on the front facing label. Consumers who have purchased the designated products are instructed to return the products to their place of purchase. Consumers may contact the company at 508-673-0111 Monday – Friday between the hours of 8am and 5pm EST.
Raw Seafoods, Inc. is working in partnership with the FDA to conduct this recall. The company is also taking the necessary steps to address this issue and apologizes for any inconvenience caused.

Natural Grocers Issues Recall on Dark Chocolate Almond Clusters

February 26, 2020

Lakewood, CO. Vitamin Cottage Natural Food Markets, Inc., a Lakewood, Colorado-based natural grocery chain, is recalling Natural Grocers brand 8 ounce Almond Clusters Dark Chocolate Non-GMO because the product contains undeclared peanut and milk allergens. People who have an allergy or severe sensitivity to peanuts or milk run the risk of serious or life-threatening allergic reaction if they consume these products. 

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Consumers who may have purchased this product are advised to discontinue use and either throw it away or return it to the store for credit or refund.

The recalled product is packaged in clear plastic bags weighing 8 ounces and bearing the “Natural Grocers” label. Pack dates between 19-178 and 20-035 are being recalled at this time.

There have been no reports of illness or injury to date, but Natural Grocers is acting out of an abundance of caution to notify consumers and recall any of the affected product in the marketplace.

UPC Code	Description	Packed on Dates
000087236088	Dark Chocolate Almond Clusters 8 oz	19-178 thru 20-035

The product was distributed to 157 Natural Grocers stores located in Arkansas, Arizona, Colorado, Iowa, Idaho, Kansas, Louisiana, Minnesota, Missouri, Montana, Nebraska, Nevada, New Mexico, North Dakota, Oklahoma, Oregon, Texas, Utah, Washington and Wyoming. 

Consumers with questions may contact the company by calling Customer Service at 303-986-4600, ext. 80801, Monday through Friday 8:00 a.m. to 5:00 p.m. (MST).

Sierra Soups Issues Allergy Alert on Undeclared Gluten in “Pasta e Fagioli” Soup

February 26, 2020

Sierra Soups of Fresno, Ca is recalling its 13 ounce packages of “Pasta e Fagioli” because the soup mix contains an individually wrapped package of pasta, which contains gluten. However outer packaging states the product is Gluten Free. People who have allergies to gluten run the risk of serious or life-threatening allergic reaction if they consume these products. 

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The recalled “Pasta e Fagioli” were distributed in Nationwide in retail stores and through mail orders.

The product comes in a 13 ounce, clear plastic package bearing the product name as well as the statement “Gluten-Free (without Pasta)”.

No illnesses have been reported to date in connection with this problem.

The recall was initiated after it was discovered that the gluten-containing product was distributed in packaging that did not clearly reveal the presence of gluten. Subsequent investigation indicates the problem was caused by a breakdown in the company’s packaging processes.

Production of the product has been suspended until FDA and the company are certain that the problem has been corrected.

Consumers who have purchased Pasta e Fagioli Soup are urged to return the product to the place of purchase for a full refund. Consumers with questions please contact the company at 1-559-387-0552 Monday-Friday 9am-5pm or info@sierrafoodsco.com.

Saratoga Potato Chips, LLC Issues Allergy Alert on Undeclared Milk in Kroger Sweet & Mesquite BBQ Potato Chips

February 20, 2020

Saratoga Potato Chips, LLC of Fort Wayne, Indiana is recalling 140 cases of Kroger Sweet & Mesquite BBQ Potato Chips 17 oz (UPC 0111100320101) with the specific lot code BEST If Used By MAY 12 20 2b5 time-stamped 18:50 to 20:55, because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk allergen run the risk of serious or life-threatening allergic reaction if they consume these products. 

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Product was distributed in Kroger stores in Michigan state, Mariano’s stores, and Roundy’s stores in Illinois state & Wisconsin state. It reached consumers through retail stores.

The product comes in a 17 oz bag marked with the lot code “BEST If Used By MAY 12 20 2b5” time-stamped 18:50 to 20:55, on the top right corner of the front of the bag. A total of 140 cases were affected.

No illnesses have been reported to date.

The issue was discovered when some consumers reported finding cheddar cheese flavored chips in the Bag of Sweet & Mesquite BBQ Potato Chips 17 oz (UPC 0111100320101) with the specific lot code BEST If Used By MAY 12 20 2b5 time-stamped 18:50 to 20:55. Saratoga Potato Chips conducted an investigation which indicated that the problem was caused by an isolated incident of human error.

Consumers who have purchased the recalled Kroger Sweet & Mesquite BBQ Potato Chips product may dispose of it or return it to their local Kroger, Mariano’s, Roundy’s stores for a full refund. Consumers with questions may contact Saratoga Potato Chips Customer Care at (905) 669-6072 x 227 during Mon-Fri, 8:00am – 5:00pm EST.

CJ Foods Voluntarily Recalls Annie Chun’s Japanese-Style Teriyaki Noodle Bowls

February 18, 2020

CJ Foods, Inc., a division of CJ America, Inc., of La Palma, CA, is voluntarily recalling Annie Chun’s Japanese-Style Teriyaki Noodle Bowls because it may contain undeclared peanuts. Use of this product may cause serious allergic reaction or illness in people who have an allergy or severe sensitivity to peanut. 

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The noodle bowls were distributed across the United States and reached consumers through retail stores and online order.

ANNIE CHUN’S JAPANESE-STYLE TERIYAKI NOODLE BOWL, 7.8 OZ, UPC CODE 7-65667-10387-6, LOT NUMBER 12/25/2020 in opaque white plastic bowl with paper sleeves

“At CJ Foods, the quality and safety of our products is our number one priority,” said Mike Smith, a spokesperson for CJ Foods. “We are working closely with the FDA on this voluntary recall to ensure the urgent notification of our retail customers and consumers. There have been no reports of illness or injury to date, but we are acting out of an abundance of caution to notify consumers and recall any of the affected product in the marketplace.”

The voluntary recall was initiated because the company discovered some bowls that were packaged in outer sleeves indicating Teriyaki Noodle Bowls contain Pad Thai noodle, which contains peanuts that are not listed on the ingredient list or allergen information.

The company has reached out to customers to cease and destroy the products that were not distributed yet and to track and destroy products already in commerce.

Consumers who have purchased an affected product should discard it and contact the company or the place of purchase for a full refund. Consumers seeking additional information can call 1-800-459-3445 from Monday – Friday, 8 am – 5 pm CT.

USDA-FSIS Recall Cases, Retail List - Update

February 13, 2020

Updated information is now available. The lists of retail consignees have been updated for recalls:

• 006-2020, Family Traditions Meat Company Recalls Ready-to-Eat Meat Stick Products Due to Misbranding and an Undeclared Allergen (Feb 8, 2020)​

Voluntary Recall Notice of Sunny Select Au Jus Gravy Mix 1 oz Pouches

February 13, 2020

McCormick & Company, Inc. is initiating a voluntary recall of Sunny Select Au Jus Gravy Mix 1 oz pouches due to an unlabeled dairy allergen. This recall does not impact any other Sunny Select products. 

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PRODUCT AND DATE CODE INFORMATION:
Product Name: Sunny Select Au Jus Gravy Mix 1 oz
UPC: 717544135500
Date Codes:
BEST BY DEC 08 2021 H
BEST BY DEC 09 2021 H

SHIPPED TO: California

McCormick & Company, Inc. has alerted Save Mart, S-Mart Foods, Lucky and FoodMaxx retailers to immediately remove the products with the affected date codes from store shelves and distribution centers.

Consumers do not need to return the product to the store where it was purchased. Instead, consumers are urged to dispose of the recalled product. Please contact Consumer Affairs at 1-800-632-5847, weekdays from 9:00 AM to 7:00 PM (Eastern Time) with inquiries.

Product being recalled will have the following labeling and best by dates of DEC 08 2021 H or DEC 09 2021 H located on back of pouch, at the bottom.

Gourmet International and Butlers Chocolates Issue Allergy Alert on Undeclared Milk

February 13, 2020                             

Gourmet International and Butlers Chocolates are recalling approximately 1900 units of the IRISH WHISKEY DARK CHOCOLATE 3.5OZ TABLET BAR because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious allergic reaction or illness if they consume these products.

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Approximately 1900 bars were distributed to a limited number of specialty food stores throughout the US (CA, CT, IN, IL, MD, MI, MN, MO, NJ, NY OH, PA, Ri, TX, WA, WI) and were available to consumers thru retail locations.

The product has the lot code 101048778 and the expiry date 08/16/2020. THE UPC IS 8-44984-17619-7

It is presented in a cream colored wrapper, measuring 6” x 3” x 3.8” and bearing the description IRISH WHISKEY – DARK CHOCOLATE WITH IRISH WHISKEY

No illnesses have been reported to date due to this occurrence.

The recall was initiated after FDA testing found high levels of milk present in the product and milk is not a listed ingredient of the product. Distribution of the product has been suspended until such time as source of the milk is determined and appropriate steps to address this issue have been taken.

Consumers who have purchased the Butlers Dark Chocolate Irish Whiskey bar may return to the place of purchase for a full refund. Consumers that have a milk allergy or individuals sensitive to milk products should not consume this product. Consumers with questions may contact either Gourmet International or Butlers Chocolates at the contact info below:

GOURMET INTERNATIONAL
PATTERSON AVENUE SE
GRAND RAPIDS, MI 49512
(Importer and Distributor)
Contact: Gayle Beld/Skye Parent
1-800-875-5557 ext 729 or 757
Gayle.Beld@Gourmetint.com
Skye.Parent@Gourmetint.com
HRS 8:30-5:30 EST

BUTLERS CHOCOLATES UC 5352
CLONSHAUGH BUSINESS PARK
DUBLIN 17, IRELAND
(Manufacturer)
Contact: KATIE BYRNE
T: +353 (1) 671-0599
katie.byrne@butlers.ie
HRS – 9:00-530 GMT ( EST + 5 HRS)​

Save A Lot Issues Allergy Alert on Undeclared Peanuts in Coburn Farms 4.5oz Sharp Yellow Cheddar Cheese, Cherry Juice

February 13, 2020

Save A Lot is recalling 131 cases of Coburn Farms 4.5oz Sharp Yellow Cheddar Cheese, Cherry Juice- Infused Dried Cranberries & Roasted Sea Salted Cashews Snackers due to a labeling error leading to undeclared peanut allergens in Snackers packages manufactured by Great Lakes Cheese Co. Inc., headquartered in Hiram, Ohio. People who have an allergy or severe sensitivity to peanuts could run the risk of a serious or life-threatening allergic reaction if they consume these products.

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The affected Snackers products were distributed through Save A Lot retail stores in the following states: Florida, Illinois, Indiana, Iowa, Kansas, Kentucky, Michigan, Mississippi, Missouri, Ohio, Tennessee, Virginia, West Virginia, Wisconsin. The Snackers have a use-by date of April 24, 2020, and product UPC code of 51933-36243 (printed on the bottom of the selling unit cardboard sleeve).

No adverse reactions have been reported to date.

The recall was initiated after it was discovered that a limited number of the Snackers contain peanuts, which, while visible through the packaging and identified on the top label of the individual Snackers tray, were not declared on the ingredient statement. This was due to an incorrect selling unit cardboard sleeve label packaged on a limited number of the Snackers.

The limited number of impacted Snackers had the incorrect selling unit cardboard sleeve of Sharp Yellow Cheddar Cheese, Cherry Juice-Infused Dried Cranberries & Roasted Sea Salted Cashews Snackers. However, the individual Snackers trays are Pepper Jack Cheese, Raisins & Honey Roasted Peanuts Snackers.

The manufacturer is actively working to address and resolve the root cause of this issue.

Consumers who have purchased the product with this specific lot code are asked to confirm they have a selling unit with an incorrect cardboard sleeve label (pictured below) and return it to the place of purchase for a full refund. Consumers or Media with questions about the recall can contact Sarah Griffin, at 314-264-7868, or by email at Sarah.Griffin@savealot.com​

Lotte Int’l America Corp Issues Allergy Alert on Undeclared Almonds in Chocopies

February 13, 2020

Lotte Int’l America Corp is recalling its 11.85-ounce packages of “Chocopie” manufactured by Lotte Confectionery Co. Ltd. Korea because of findings of a small amount of almond in the product and packaging shows the “manufactured in a facility that also processes peanut & almond”.

Since Lotte Int’l America Corp. is very well aware of the severe consequences of allergen reaction to almonds, we voluntarily initiated recall procedure right after discovery of the problem. People who have an allergy or severe sensitivity specific to peanut and almonds run the risk of serious or life-threatening allergic reaction if they consume products containing the allergen. 

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The recalled “Chocopie” were distributed nationwide in retail stores and online stores. The recalled “Chocopie” product varies in three different packages & expiration dates.

This is to inform you of a product recall involving:

Chocopie Original 12pk (Exp: 06/23/2020)

Chocopie Banana 12pk (Exp: 04/11/2020)

Chocopie Cacao 12pk (Exp: 04/23/2020)

The Chocopie Original 12pk comes in a 11.85-ounce, plastics wrap package within a paper carton package marked with UPC code # 8801062160709 on the side and with an expiration date of 06/23/20 stamped on the side. The Chocopie Banana 12pk comes in a 11.85-ounce, package marked with UPC code # 845502061407 on the side and with an expiration date of 04/11/20 stamped on the side. The Chocopie Cacao 12pk comes in a 11.85-ounce, package marked with UPC code # 8801062475148 on the side and with an expiration date of 04/23/20 stamped on the side.

The company are certain that the problem has been corrected and no illnesses have been reported to date in connection with this problem.

LOTTE Int’l America Corp is working fully in partnership with FDA to fully investigate the matter and comply with all necessary recall procedures. The Company is also taking the necessary steps to address this issue and apologizes for any inconvenience caused by this product issue.

Consumers who have purchased 11.85-ounce packages of ” Chocopie Original, Banana, Cacao flavors” with expiration dates specified above are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-213-688-8806 (Monday – Friday 8:00am to 5:00 pm PST).​