Food Recalls

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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

More Information

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
 

More Information

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
 

More Information

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
 

More Information

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
 

More Information

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
 

More Information

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. 

More Information

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. 

More Information

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. 

More Information

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. 

More Information

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. 

More Information 

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.

More Information

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.

More Information

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. 

More Information

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).​