Food Recalls | Harvest Hope

Mondelēz Global LLC Conducts Voluntary Recall of Two Varieties of belVita Breakfast Sandwich Products Sold in the United States Due to Undeclared Peanut Allergen

July 3, 2023

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Mondelēz Global LLC announced today a voluntary recall of two varieties of belVita Breakfast Sandwich products, manufactured in the United States and sold nationwide, due to the possibility that the products may contain undeclared peanut resulting from cross-contact on a single manufacturing line. People who have an allergy or severe sensitivity to peanut may risk serious or life-threatening allergic reactions by consuming these products.

This recall is limited exclusively to the belVita Breakfast Sandwich products listed in the grid below, available at retail stores nationwide. No other belVita products, Mondelēz Global LLC products, or markets outside the United States are included in or affected by this recall.

Product Description	Retail UPC	Best When Used By Date
belVita Breakfast Sandwich, Dark Chocolate Creme variety (8.8 oz carton)	0 44000 04328 5	All Best When Used by Dates prior to and including February 25, 2024 (Located on top flap of carton)
belVita Breakfast Sandwich, Dark Chocolate Creme variety (14.08 oz carton)	0 44000 05723 7	All Best When Used by Dates prior to and including February 25, 2024 (Located on side of carton)
belVita Breakfast Sandwich, Dark Chocolate Creme variety (1 lb 5.12 oz carton)	0 44000 05861 6	All Best When Used by Dates prior to and including February 25, 2024 (Located on side flap of carton)
belVita Breakfast Sandwich, Dark Chocolate Creme variety (14.08 oz carton)	0 44000 06330 6	All Best When Used by Dates prior to and including February 25, 2024 (Located on side of carton)
belVita Breakfast Sandwich, Dark Chocolate Creme variety (2 lb 12 oz carton)	0 44000 04602 6	All Best When Used by Dates prior to and including February 25, 2024 (Located on side of carton)
belVita Breakfast Sandwich, Cinnamon Brown Sugar with Vanilla Creme variety (8.8 oz carton)	0 44000 06304 7	All Best When Used by Dates prior to and including February 25, 2024 (Located on top flap of carton)
belVita Breakfast Sandwich, Dark Chocolate Creme variety (1.76 oz pouch)	0 44000 04070 3	All Best When Used by Dates prior to and including February 25, 2024 (Located on back of pouch)
belVita Breakfast Sandwich, Cinnamon Brown Sugar with Vanilla Creme variety (1.76 oz pouch)	0 44000 06370 2	All Best When Used by Dates prior to and including February 25, 2024 (Located on back of pouch)

We became aware of this issue during an internal manufacturing inspection, when we found the potential presence of peanut protein residue on the line used to make these products. There have been three unconfirmed reports of possible allergic reaction to date related to these products.

Consumers who have a peanut allergy should not eat these products and should discard any product identified in the grid above they may have. Consumers can contact the company at 1-855-535-5948, 24 hours a day, for more information about the recall, and Consumer Relations specialists are available Monday-Friday, 9am to 6pm EST (excluding July 4, 2023).

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/mondelez-global-llc-conducts-voluntary-recall-two-varieties-belvita-breakfast-sandwich-products-sold

Panamerican Foods, LLC Recalls Ineligible Pork and Beef Bean Stew Products Imported from Brazil

June 30, 2023

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Panamerican Foods, LLC, a distributor and importer of record located in Kearny, N.J., is recalling approximately 4,978 pounds of the pork and beef bean stew products that were imported from an establishment in Brazil that is not eligible to export meat products to the United States, U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The following products are subject to recall, regardless of the product date [view labels]:

430g cans containing “Anglo Feijoada Pronta para servir”.
430g cans containing “Bordon Feijoada PRONTO PARA SERVIR”.

The products subject to recall bear establishment number “76 S.I.F.” on the can. These items were shipped to retail locations nationwide.

The problem was discovered when FSIS followed up on a referral from USDA’s Smuggling Interdiction and Trade Compliance Program. The pork and beef bean stew products, which were imported from a Brazilian establishment not eligible to export meat products to the United States, were observed for sale in a retail store.

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 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 Carlos Albarracin, President of Panamerican Foods, LLC, at 917-544-8237 or email at carlospanamerican@aol.com.

https://www.fsis.usda.gov/recalls-alerts/panamerican-foods-llc-recalls-ineligible-pork-and-beef-bean-stew-products-imported

House of Raeford Recalls Foster Farms Brand Mini Chicken Corn Dog Products Due to Possible Spoilage

June 30, 2023

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House of Raeford, a Nesmith, S.C., establishment, is recalling approximately 76,961 pounds of corn dog products due to possible spoilage, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The mini chicken corn dogs were produced on April 24, 2023. The following product is subject to recall [view labels]:

1.83-lb. resealable bag containing “FOSTER FARMS MINI CORN DOGS BITE-SIZED CHICKEN FRANKS DIPPED IN BATTER HONEY CRUNCHY FLAVOR” with lot codes 123114 and 223114 and best if used by date of 4/23/24.

The product subject to recall bears the establishment number “P- 9136” printed on the package. These items were shipped to retail locations nationwide.

The problem was discovered after the firm notified FSIS that it received consumer complaints that the product had an odor, off appearance, and unpleasant taste.

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 and members of the media with questions about the recall can contact Dave Witter, House of Raeford Corporate Communications Manager, at 910-282-7179 or email at dave.witter@houseofraeford.com.

https://www.fsis.usda.gov/recalls-alerts/house-raeford-recalls-foster-farms-brand-mini-chicken-corn-dog-products-due-possible

Townsend Farms Inc. Voluntarily Recalling Specific Frozen Fruit Products Because of Possible Listeria monocytogenes Contamination

June 28, 2023

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Townsend Farms Inc. of Fairview, Oregon out of an abundance of caution is voluntarily recalling specific frozen fruit products linked to mango chunks supplied by SunOpta (Sunrise Growers) due to potential Listeria monocytogenes contamination.

Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. Any consumers concerned about an illness should contact their physician.

The product was distributed to Kroger Stores in the following states: Alabama, Arkansas, Georgia, Illinois, Indiana, Kentucky, Louisiana, Michigan, Missouri, Mississippi, Ohio, South Carolina, Tennessee, Texas, Virginia, and West Virginia; and under the following banners: Baker’s, Dillons, Food 4 Less, FoodsCo, Fry’s, Gerbes, Jay C, Mariano's, Metro Market, Pay Less, Pick n’ Save, Ralphs, Ruler, and Smith’s from November 06, 2022 to March 16, 2023.

This voluntary recall includes the following products date codes. Date codes can be found printed on the back panel of the packaging.

UPC 0 11110 84663 1 Private Selection 48oz Tropical Mango Chunks
- Date Codes:
  - BEST IF USED BY 04/30/24 T1 PRODUCT OF MEXICO F2202171
  - BEST IF USED BY 04/30/24 T2 PRODUCT OF MEXICO F2202172
  - BEST IF USED BY 04/30/24 T1 PRODUCT OF MEXICO F2202182
  - BEST IF USED BY 04/30/24 T2 PRODUCT OF MEXICO F2202183
  - BEST IF USED BY 05/04/24 T1 PRODUCT OF MEXICO F2202225
  - BEST IF USED BY 05/04/24 T1 PRODUCT OF MEXICO F2202229
  - BEST IF USED BY 05/07/24 T4 PRODUCT OF MEXICO F2202236
  - BEST IF USED BY 05/07/24 T4 PRODUCT OF MEXICO F2202241
  - BEST IF USED BY 07/18/24 T3 PRODUCT OF MEXICO F2300116
UPC 0 11110 87853 3 Private Selection 16oz Strawberry, Mango & Pineapple Blend
- Date Codes:
  - BEST IF USED 04/30/24 T4 PRODUCT OF USA, MEXICO & COSTA RICA F2202174
  - BEST IF USED 04/30/24 T4 PRODUCT OF USA, MEXICO & COSTA RICA F2202185
  - BEST IF USED 05/04/24 T2 PRODUCT OF USA, COSTARICA & MEXICO F2202227
  - BEST IF USED 05/28/24 T2 PRODUCT OF PERU, MEXICO & COSTA RICA F2202332
UPC 0 11110 82026 6 Private Selection 48oz Classic Fruit Medley
- Date Codes:
  - BEST IF USED 05/03/24 T3 PRODUCT OF USA, MEXICO, CHILE & COSTARICA F2202213
  - BEST IF USED 05/03/24 T3 PRODUCT OF USA, MEXICO, CHILE & COSTA RICA F2202220
  - BEST IF USED 05/04/24 T3 PRODUCT OF USA, MEXICO, CHILE & COSTA RICA F2202226
  - BEST IF USED 05/04/24 T3 PRODUCT OF USA, MEXICO, CHILE & COSTA RICA F2202230
  - BEST IF USED 05/10/24 T3 PRODUCT OF USA, MEXICO, PERU, CHILE & COSTA RICA F2202268
  - BEST IF USED 05/10/24 T3 PRODUCT OF USA, MEXICO, PERU, CHILE & COSTA RICA F2202273
  - BEST IF USED 05/18/24 T3 PRODUCT OF USA, MEXICO, CHILE, PERU & COSTA RICA F2202319
  - BEST IF USED 05/18/24 T3 PRODUCT OF USA, MEXICO, CHILE, PERU & COSTA RICA F2202325
UPC 0 11110 89623 0 Private Selection 48oz Blueberries, Strawberries & Mangoes
- Date Codes:
  - BEST IF USED 04/30/24 T3 PRODUCT OF USA & MEXICO F2202173
  - BEST IF USED 04/30/24 T3 PRODUCT OF USA & MEXICO F2202184
  - BEST IF USED 05/07/24 T3 PRODUCT OF USA & MEXICO F2202235
  - BEST IF USED 05/07/24 T3 PRODUCT OF USA & MEXICO F2202240
  - BEST IF USED 05/08/24 T6 PRODUCT OF USA & MEXICO F2202247

The affected retail customers have been notified of this recall and instructed to remove any recalled product from retail store shelves and inventories.

Customers are urged to check their freezers for the recalled product, not to consume it and either discard the product or return it to the store for a full refund. Consumers may also request a refund by calling Kroger Customer Connect at 800-632-6900, Option 1, Monday through Friday, 7 a.m.- Midnight, EST. Saturday-Sunday, 7 a.m.-9:30 p.m., EST.

Consumers seeking product information may email recalls@townsendfarms.com or call 503-512-1317. Monday through Friday, 7 a.m.-Midnight, EST; Saturday-Sunday, 7 a.m.-9:30 p.m., EST.

To date, there have been no illnesses associated with this voluntary recall.

This voluntary recall is being conducted with the knowledge of the U.S. Food and Drug Administration (FDA).

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/townsend-farms-inc-voluntarily-recalling-specific-frozen-fruit-products-because-possible-listeria

Foremost Foods Corporation Voluntarily Recalls Pamana Brand Mini Fruit Jelly Cup (35.27OZ) Because of Potential Choking Hazard

June 26, 2023

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FOREMOST FOODS CORPORATION OF POMONA, CA is voluntarily recalling its MINI FRUIT JELLY CUP (35.27oz.) due to the products being a potential choking hazard based off the product size. Small jelly cups have previously been implicated in choking deaths of children.

The recalled jelly cups were distributed nationwide in Seafood City supermarkets and are sold in large clear jars. Below are the products being recalled:

Pamana Mini Fruit Jelly Cup (Assorted Flavors); UPC 795981293038; Net Weight 35.27 oz.
Pamana Mini Fruit Jelly Cup (Mango Flavor); UPC 795981293045; Net Weight 35.27 oz.
Pamana Mini Fruit Jelly Cup (Lychee Flavor); UPC 795981293021; Net Weight 35.27 oz.

No incidents of consumers choking have been reported to date in connection with these products.

The potential choking hazard was confirmed after discussion with a representative from the Food and Drug Administration.

Consumers who have purchased the above products are urged to return them to the store of purchase for a full refund or dispose them in a sealed package inside a secure garbage can with a tight‐fitting lid. For more information or inquiries, please contact the company at (909)‐525‐9500 Monday thru Friday between 9 am and 5 pm PST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/foremost-foods-corporation-voluntarily-recalls-pamana-brand-mini-fruit-jelly-cup-3527oz-because

Santo’s Frozen Foods, Inc. Issues Allergy Alert on Undeclared Milk and Sesame Seeds on Mislabeled Deviled Crabs Cases

June 23, 2023

More Information: Santo’s Frozen Foods, Inc. issued a voluntary recall of select boxes of 100 count, 36 count, and 24 count boxes of Deviled Crabs because they contain undeclared milk and sesame seeds. People with an allergy or severe sensitivity to milk or sesame seeds run the risk of a serious or life-threatening allergic reaction if they consume these products.

Recalled product was distributed and available for purchase from March through June 2023.

The Deviled Crabs under recall are packaged in plain brown cardboard boxes with two white labels. The recalled products have a six digit Lot # starting with 23 and ending with 03 or 04 or 05. The Lot # is on a white label on the long side of the box.

The recall was initiated after it was found that the affected box labels do not declare milk or sesame seeds as allergens.

No allergic reactions related to this matter have been reported to date. Consumers with an allergy or severe sensitivity to milk or sesame seeds should not consume the product and discard it immediately. Santo’s Frozen Foods, Inc. has informed the FDA of this action.

Consumers with the product described can contact Santo’s Frozen Foods, Inc. at (813)875-4901 (7am-3pm EST, Monday-Friday.)

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/santos-frozen-foods-inc-issues-allergy-alert-undeclared-milk-and-sesame-seeds-mislabeled-deviled

Voluntary Recall of Specific Frozen Fruit Products Due to Possible Contamination by Listeria monocytogenes

June 21, 2023

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SunOpta Inc’s subsidiary, Sunrise Growers Inc., has issued a voluntary recall of specific frozen fruit products linked to pineapple provided by a third-party supplier due to the potential for these products to be contaminated with Listeria monocytogenes.

Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. Any consumers concerned about an illness should contact a physician.

Products were distributed via the following retailers:

Walmart: Great Value Mixed Fruit, Great Value Dark Sweet Cherries, and Great Value Mango Chunks sold at stores in AR, AZ, CA, CO, DC, IA, ID, IL, IN, KS, KY, LA, MD, MN, MO, MT, ND, NE, NM, NV, OH, OK, OR, PA, SD, TX, UT, VA, WV and WY from January 19, 2023 to June 13, 2023
Whole Foods: 365 Organic Tropical Fruit Medley, 365 Organic Pineapple Chunks, 365 Pineapple Chunks, 365 Organic Whole Strawberries, 365 Organic Slice Strawberries and Bananas, and 365 Organic Blackberries distributed to select stores throughout the US from November 1, 2022 to June 21, 2023
Trader Joe’s: Trader Joe’s Organic Tropical Fruit Blend distributed to select distribution centers or stores in AK, AL, CT, CO, DE, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NE, NH, NJ, NM, NY, OH, OK, PA, RI, TN, TX, VA, VT, WI, and Washington DC from March 28, 2023 to April 11, 2023
Target: Good & Gather Organic Cherries and Berries Fruit Blend, Good & Gather Dark Sweet Whole Pitted Cherries, Good & Gather Mango Strawberry Blend, Good & Gather Mixed Fruit Blend, Good & Gather Mango Chunks, Good & Gather Blueberries, and Good & Gather Triple Berry Blend distributed nationwide from October 14, 2022 to May 22, 2023
Aldi: Season’s Choice Tropical Blend distributed to select distribution centers or stores in AL, AR, CT, FL, GA, IA, KS, KY, MA, MD, MI, MO, MS, NC, NE, NH, NY, OH, OK, PA, RI, SC, TN, TX, VA, VT and WV from October 11, 2022 to May 22, 2023
AWG (Associated Wholesale Grocers): Best Choice Pitted Red Tart Cherries Unsweetened distributed to select distribution centers or stores in KS, MO, NE and OK from April 5, 2023 to May 4, 2023

To date, there have been no illnesses associated with this voluntary recall.

Consumers are urged to check their freezers for the recalled product, not to consume it and either discard the product or return it to the store for a full refund. All other Sunrise Growers products that have different lot codes or best by dates are not affected by this recall. The affected retail customers have been notified of this recall and instructed to remove any recalled product from retail store shelves and inventories.

Consumers seeking information may email recall@sunrisegrowers.com or call 1.888.490.5591 Monday through Friday, 8:00 a.m. to 5:00 p.m. Pacific Time.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration (FDA).

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-specific-frozen-fruit-products-due-possible-contamination-listeria-monocytogenes

Frito-Lay Issues Allergy Alert on Undeclared Milk in Mislabeled Tostitos Avocado Salsa Jar Dip

June 16, 2023

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Frito-Lay today issued a voluntary recall of select 15 oz. Tostitos Avocado Salsa Jar Dips that may contain an undeclared milk allergen. Those with an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume these products.

While the front of the affected jar is correctly labeled as Tostitos Avocado Salsa, the back of the jar is mislabeled with another product’s nutrition information and declarations. As a result, the allergen milk is not declared on the label.

The product covered by this recall was distributed nationwide at retail stores and via e-commerce channels. Consumers would have been able to purchase the jars as early as April 5, 2023.

No other Tostitos products, flavors, sizes, or dip variety packs are recalled.

No allergic reactions related to this matter have been reported to date. If consumers have an allergy or severe sensitivity to milk, they should not consume the product and discard it immediately. Frito-Lay has informed the FDA of this action.

Consumers with the product described below can contact Frito-Lay Consumer Relations at 1-800-352-4477 (9 a.m. – 4:30 p.m. CST, Monday-Friday).

The specific recalled product information is listed below:

Product	Size	Front Label/Representative Image	UPC	Best Before Date
Tostitos Avocado Salsa Dip packaged in a glass jar	15 oz. 425.2 grams	Please see images below	UPC barcode ending in 05597 Please see images below	Located on upper rim of jar: 2 NOV 23 OR 3 NOV 23

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/frito-lay-issues-allergy-alert-undeclared-milk-mislabeled-tostitos-avocado-salsa-jar-dip

Richin Trading Inc. Voluntarily Recalls Sunwave Brand Mini Fruit Jelly Cup (35.27oz./52.90oz) Because of Potential Choking Hazard

June 16, 2023

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RICHIN TRADING INC. OF ALHAMBRA, CA is voluntarily recalling its MINI FRUIT JELLY CUP (35.27oz. and 52.90 oz.) due to the products being a potential choking hazard based off the product size. Small jelly cups have previously been implicated in choking deaths of children.

The recalled jelly cups were distributed nationwide in retail food stores and are sold in large clear jars. Below are the products being recalled:

Sun Wave Mini Fruit Jelly Cup (Assorted Flavors); UPC 715685121437; Net Weight 52.91 oz.
Sun Wave Mini Fruit Jelly Cup (Mango Flavor); UPC 715685121444; Net Weight 52.91 oz.
Sun Wave Mini Fruit Jelly Cup (Lychee Flavor); UPC 715685121451; Net Weight 52.91 oz.
Sun Wave Mini Fruit Jelly Cup (Assorted Flavors); UPC 715685121512; Net Weight 35.27 oz.
Sun Wave Mini Fruit Jelly Cup (Lychee Flavor); UPC 715685121529; Net Weight 35.27 oz.
Sun Wave Mini Fruit Jelly Cup (Mango Flavor); UPC 715685121536; Net Weight 35.27 oz

No incidents of consumers choking have been reported to date in connection with these products.

The potential choking hazard was confirmed after discussion with a representative from the Food and Drug Administration.

Consumers who have purchased the above products are urged to return them to the store of purchase for a full refund or dispose them in a sealed package inside a secure garbage can with a tight-fitting lid. For more information or inquiries, please contact the company at (626)-308-3212 Monday thru Friday between 9 am and 5 pm PST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/richin-trading-inc-voluntarily-recalls-sunwave-brand-mini-fruit-jelly-cup-3527oz5290oz-because

Conagra Brands, Inc., Recalls Frozen Beef Shepherd’s Pie Products Due to Possible Foreign Matter Contamination

June 16, 2023

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Conagra Brands, Inc., a Russellville, Ark. establishment, is recalling approximately 2,717 pounds of frozen beef shepherd’s pie products that may be contaminated with extraneous materials, specifically clear, flexible plastic, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The frozen beef shepherd’s pie products were produced on March 1, 2023, with time stamps ranging between 17:45-17:56 hours. The following products are subject to recall [view labels]:

4.31 lbs. cases of “MC Beef Shepherd’s Pie” with lot code 5006306020, BEST BY FEB 24 2024 and case code 2113100032, containing six 11.5 oz. carton packages of "Marie Callender’s BEEF SHEPHERD’S PIE” with lot code 5006306020 and BEST BY FEB 24 2024 on the side panel, with time stamps ranging between 17:45-17:56

The products subject to recall bear establishment number “EST 233” next to the USDA mark of inspection on the case and above the “BEST BY DATE” on the side panel of the individual product. These items were shipped to retail customer distribution centers in California, Colorado, Oregon, and Utah, and further distributed nationwide.

The problem was discovered when the firm received consumer complaints reporting pieces of clear, flexible plastic in the product, and notified FSIS of the situation.

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’s Consumer Care Hotline at 877-469-3783 or consumer.care@conagra.com. Members of the media with questions about the recall can contact Dan Hare, Sr. Director of Corporate Communications, Conagra at 312-549-5355 or Daniel.hare@conagra.com.

https://www.fsis.usda.gov/recalls-alerts/conagra-brands-inc--recalls-frozen-beef-shepherds-pie-products-due-possible-foreign

Gelato Boy Issues Allergy Alert on Undeclared Milk in Chocolate Chunk Gelato

June 14, 2023

More Information: Gelato Boy of Boulder, Colorado is recalling 728 cases / 5,824 units of Chocolate Chunk Gelato because it may contain undeclared MILK. People who have an allergy or severe sensitivity to MILK run the risk of serious or life-threatening allergic reaction if they consume this product.

Gelato Boy Chocolate Chunk was distributed nationwide and is sold at grocery stores, including but not limited to Sprouts Farmer’s Market, King Soopers / City Market, Whole Foods Market and others. The product can be found in the ice cream and novelties aisle.

The product is labeled “CHOCOLATE CHUNK GELATO” and comes in a 16 fl oz paper pint container with a lid. The affected Lot Code is 4043T2, with a Best By date of 04/25. The UPC is 853457008002.

No illnesses have been reported to date.

The recall was initiated after a customer notified Gelato Boy that the pint did not have its normal appearance and that it “tasted like there’s dairy in it”. Gelato Boy immediately located a pint with the same lot code and brought it to a lab for testing. It was confirmed that the product containing MILK was distributed in packaging that did not reveal the presence of MILK.

This recall is being made with the knowledge of the U.S. Food and Drug Administration.

Customers with a MILK allergy or sensitivity who have purchased the affected product are urged not to consume the product and dispose of it or return it to their place of purchase for a full refund.

Consumers with questions may contact the company at 720-548-0416, or at spoon@gelatoboy.com from 8am-4:30pm MST, Monday-Friday.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gelato-boy-issues-allergy-alert-undeclared-milk-chocolate-chunk-gelato?utm_medium=email&utm_source=govdelivery

J.T.M. Provisions Company Recalls Ready-To-Eat Homestyle Chili Topping Product Due to Misbranding and an Undeclared Allergen

June 9, 2023

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J.T.M. Provisions Company, a Harrison, Ohio establishment, is recalling approximately 200 pounds of ready-to-eat (RTE) chili topping 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 labeled as chili topping may actually contain beef taco filling, which contains soy, a known allergen, that is not declared on the product label.

The frozen, RTE Homestyle Chili Topping packages, which may actually contain beef taco filling, were produced March 14, 2023, and packed inside cases labeled as beef taco filling. The following product is subject to recall [view label]:

5-lb. boilable plastic bags of “Gordon Choice® Homestyle Chili Topping” with lot code 230732002.

The product subject to recall bears establishment number “1917A” inside the USDA mark of inspection. This item was shipped to institutional and retail locations nationwide.

The problem was discovered when the producing establishment notified FSIS that it had received a consumer complaint that bags labeled as homestyle chili topping contained beef taco filling.

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 institutional or consumers’ freezers. Consumers who have purchased these products are urged not to consume them and institutions are urged not to serve these products. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution lists will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers and members of the media with questions about the recall can contact Matt Montgomery, Chief Financial Officer, J.T.M. Provisions Company, at 513-367-4900, Ext. 117 or mmontgomery@jtmfoodgroup.com.

https://www.fsis.usda.gov/recalls-alerts/j-t-m--provisions-company-recalls-ready-eat-homestyle-chili-topping-product-due

T.W. Garner Food Company Issues Voluntary Recall on Texas Pete® Buffalo Wing Sauce Due to Undeclared Soy

May 25, 2023

More Information: T.W. Garner Food Company is voluntarily recalling 50,688 bottles of 12 oz. Texas Pete® Buffalo Wing Sauce with best used by 120623T 065239 UPC 0 75500 10011 6 because some of the bottles may contain Texas Pete® Extra Mild Wing Sauce which contains 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 product.

The product can be identified as a 12 oz. glass bottle with orange sauce, called Texas Pete® Buffalo Wing Sauce. The only product affected has best used by 120623T 065239 printed on the cap of the product.

No illnesses have been reported to date.

The recall was initiated after a report was received from a direct customer that a bottle labeled as Texas Pete® Buffalo Wing Sauce was located instead of Texas Pete® Extra Mild Wing Sauce. The bottle of Texas Pete® Buffalo Wing Sauce was missing the allergen declaration of soy. Investigation indicates the problem was caused by applying the wrong label during a portion of the production run.

Product was shipped to distribution centers and retail stores located in AL, CT, FL, GA, LA, MS, NC, NY, PA, SC, TN, TX & VA. Consumers with a soy allergy or sensitivity who have purchased Texas Pete® Buffalo Wing Sauce with a best used by 120623T 065239 with a UPC 0 75500 10011 6 are urged not to consume the product and dispose of it or return it to their place of purchase for a full refund.

Consumers with questions may contact Mrs. Katerine Cardoso, Quality Assurance Manager at (336) 231-6417 Monday - Friday 8:00 am - 6:00 pm EST or email at ContactUs@garnerfoods.com.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tw-garner-food-company-issues-voluntary-recall-texas-peter-buffalo-wing-sauce-due-undeclared-soy?utm_medium=email&utm_source=govdelivery

Van Leeuwen Issues Voluntary Recall on Undeclared Walnuts in its Brown Sugar Chunk Ice Cream Pints

May 23, 2023

More Information: Van Leeuwen Ice Cream of Brooklyn, NY is voluntarily recalling 4,096 frozen 14 oz pints of its French Ice Cream product "Brown Sugar Chunk” because it contains an undeclared allergen, walnuts. People who have an allergy or severe sensitivity to walnuts run the risk of serious or life-threatening allergic reaction if they consume these products.

The recalled products are distributed nationally in retail stores. The product comes in a 14-ounce reddish brown package with black lettering on the cup and lid, as reflected in the image below. The product is marked with lot number 23P102 (Best By Date April 12, 2025) which is displayed on the bottom of the pint. The recall does not apply to any other lot marking, best by date, or varieties of Van Leeuwen Ice Cream products.

The recall was voluntarily initiated after a customer complaint led to the discovery that the ice cream in this lot contains walnuts but was distributed in packaging that did not declare the presence of walnuts. The cause of the product labeling error is being investigated.

Consumers who have purchased the impacted lot should return them to the place of purchase for a full refund.

Any questions or concerns should be directed to JD Dillion, JD@vanleeuwenicecream.com or 215.824.6613 between the hours of 9:00 – 5:00 EST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/van-leeuwen-issues-voluntary-recall-undeclared-walnuts-its-brown-sugar-chunk-ice-cream-pints?utm_medium=email&utm_source=govdelivery

Hu Products Issues Voluntary Allergy Alert on Undeclared Tree Nuts (Hazelnut, Cashew, and/or Almond) in Vanilla Crunch Dark Chocolate Bar Product in the U.S.

May 18, 2023

More Information

Hu Products announced today a voluntary recall in the United States of a single production lot of Vanilla Crunch Dark Chocolate Bar product (2.1 oz bar) because some packages may potentially contain undeclared hazelnut, cashew, and/or almond that were inadvertently added to the product during manufacturing. People who are sensitive or have allergies to hazelnut, cashew, and/or almond could be at risk of a serious or life-threatening allergic reaction if they consume this product.

This recall is limited to one lot code (L2343C) of the Hu Vanilla Crunch Dark Chocolate Bar (2.1 oz. bar), which was sold nationwide in retail stores and online in the United States. No other Hu products are affected by this recall.

The product being recalled is the following:

Product Description: Vanilla Crunch Dark Chocolate Bar
Item UPC: 850180006206
Lot Code & Best By Date: L2343C - 12/09/2024

A picture of the consumer package label is shown below.

There have been no adverse events reported to Hu Products to date in connection with this product to date.

Consumers who are sensitive or have allergies to hazelnut, cashew, and/or almond should not eat this product and should discard any product they may have. Consumers should contact the company at 1-855-535-5948 to get more information about the recall. The information line is open 24 hours a day and Consumer Relations specialists are available Monday-Friday, 8 a.m. to 5 p.m. Central Time.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hu-products-issues-voluntary-allergy-alert-undeclared-tree-nuts-hazelnut-cashew-andor-almond-vanilla?utm_medium=email&utm_source=govdelivery

Eastern Meat Solutions, Inc. Recalls Raw, Boneless Pork Products Imported without Benefit of Import Reinspection

May 12, 2023

More Information

Eastern Meat Solutions, Inc., the importer of record located in Ontario, Canada, is recalling approximately 40,763 pounds of raw, boneless pork products that were not presented for import reinspection into the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The raw, boneless pork products were imported from Canada, and further processed by another company into barbeque pork products. The following products are subject to recall [view labels]:

16-oz. plastic packages containing Park Street Deli “SWEET CHIPOTLE Boneless Pork Ribs with Sauce” with Lot # 3115, Use By 07/08/23; Lot # 3123, Use By 07/17/23; or Lot #3114, Use By 07/08/23 on the packages.
16-oz. plastic packages containing Park Street Deli “HAWAIIAN STYLE Boneless Pork Ribs with Sauce” with Lot # 3115, Use By 07/08/23; Lot # 3123, Use By 07/17/23; or Lot #3114, Use By 07/08/23 on the packages.
16-oz. plastic packages containing “marketside READY TO HEAT BBQ PORK BURNT ENDS” with Lot #3116, Use By 08/29/23; Lot #3117, Use By 08/30/23; or Lot #3122, Use By 09/04/23 on the packages.

The products subject to recall bear establishment number “EST. 4800” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.

The problem was discovered by FSIS inspection personnel who determined that the products were not presented for 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 www.fsis.usda.gov/recalls.

Consumers and members of the media with questions about the recall can contact Eastern Meat Solutions at customer.service@sierrascs.com.

https://www.fsis.usda.gov/recalls-alerts/eastern-meat-solutions-inc--recalls-raw-boneless-pork-products-imported-without

Mitten Gourmet, LLC, Recalls Ready-to-Eat Pork Rind Products Produced without Benefit of Inspection

May 10, 2023

More Information

Mitten Gourmet, LLC, a Freeland, Michigan establishment, is recalling approximately 1,137 pounds of ready-to-eat pork rind 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 pork rind products of various flavors were produced on various dates from September 9, 2021, through May 5, 2023. The following products are subject to recall [view labels]:

2.0-oz. clear bags containing Mitten Gourmet “PARMESAN GARLIC Pork Rinds”
2.0-oz. clear bags containing Mitten Gourmet “PIZZA Pork Rinds”
2.0-oz. clear bags containing Mitten Gourmet “BUFFALO Pork Rinds”
2.0-oz. clear bags containing Mitten Gourmet “NACHO CHEESE Pork Rinds”
2.0-oz. clear bags containing Mitten Gourmet “JALAPENO Pork Rinds”
2.0-oz. clear bags containing Mitten Gourmet “HONEY MUSTARD Pork Rinds”
2.0-oz. clear bags containing Mitten Gourmet “DILL PICKLE Pork Rinds”
2.0-oz. clear bags containing Mitten Gourmet “BARBECUE Pork Rinds”
2.0-oz. clear bags containing Mitten Gourmet “SALT N PEPPER Pork Rinds”

The products subject to recall do not bear the USDA mark of inspection because Mitten Gourmet, LLC, is not a federally inspected establishment. These items were shipped to retail locations nationwide.

The problem was discovered during routine FSIS surveillance activities when the ready-to-eat pork rind products were observed for sale without the USDA mark of inspection. FSIS determined that the producer is not an FSIS-inspected facility.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.

FSIS is concerned that some product may be in consumers’ pantries. 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 Miquel Varney, CEO of Mitten Gourmet, LLC, at 989-402-5372 or Support@Mittengourmet.com.

https://www.fsis.usda.gov/recalls-alerts/mitten-gourmet-llc-recalls-ready-eat-pork-rind-products-produced-without-benefit

Bakkavor USA Issues Allergy Alert on Undeclared Milk and Walnuts in Trader Joe’s Genova Pesto

May 9, 2023

More Information: Bakkavor USA is issuing a voluntary recall of Trader Joe’s Genova Pesto (SKU# 15759) because the product may contain undeclared milk and walnuts. People who have an allergy or severe sensitivity to milk or walnuts run the risk of serious or life-threatening allergic reactions if they consume this product.

The impacted product has UPC 0015 7353 on the side label and Use By date of 05/27/2023 with a time stamp between 06:28 – 07:07 printed on the bottom of the tub, was distributed to Trader Joe’s stores between 4/28/2023 and 4/30/2023 in Alabama, Arizona, California, Florida, Georgia, Idaho, Nevada, North Carolina, Oregon, South Carolina, Tennessee, Utah, Virginia, and Washington.

The recall was initiated after it was discovered at a retail store that the Genova Pesto was mistakenly packaged into tubs marked "Hummus Dip”. These tubs do not contain an allergen declaration of milk or walnuts, which are both found in the Genova Pesto.

No illnesses or allergic reactions have been reported to date, and all potentially impacted product has been removed from sale. An investigation into the root cause of this error is ongoing.

This recall is being made with the knowledge of the U.S. Food and Drug Administration.

Consumers who have purchased or received any donations of Trader Joe’s Genova Pesto and have a milk or walnut allergy are urged not to consume the product and to discard or return it to any Trader Joe’s for a full refund. Consumers with questions may contact Bakkavor USA at (855) 321-7504 between the hours of 9am to 4 pm Eastern.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bakkavor-usa-issues-allergy-alert-undeclared-milk-and-walnuts-trader-joes-genova-pesto?utm_medium=email&utm_source=govdelivery

General Mills Recalls Four Gold Medal Unbleached and Bleached All Purpose Flour Varieties Dated March 27, 2024 and March 28, 2024

April 28, 2023

More Information

General Mills today announced a voluntary national recall of two-, five- and 10-pound bags of its Gold Medal Unbleached and Bleached All Purpose Flour with a “better if used by” date of March 27, 2024, and March 28, 2024. The recall is being issued for the potential presence of Salmonella Infantis, which was discovered during sampling of the five-pound bag product.

This recall affects two date codes of Gold Medal Unbleached All Purpose Flour in the five- and ten pound bags and two date codes of Gold Medal Bleached All Purpose Flour in the two- and five-pound bags. All other types of Gold Medal Flour are not affected by this recall.

Consumers are asked to check their pantries and dispose of the product affected by this recall. Consumers who have had to discard products covered by this recall may contact General Mills Consumer Relations at 1-800-230-8103.

Guidance from the Food and Drug Administration(FDA) and the Centers for Disease Control(CDC) warn that consumers should refrain from consuming any raw products made with flour. Salmonella Infantisis killed by heat through baking, frying, sautéing or boiling products made with flour. All surfaces, hands and utensils should be properly cleaned after contact with flour or dough.

This voluntary recall includes the following code dates currently in stores or consumers’ pantries:

Gold Medal Unbleached All Purpose 5LB Flour
- Package UPC: 000-16000-19610
- Recalled Better if Used By Date: 27 Mar 2024 and 28 March 2024
Gold Medal Unbleached All Purpose 10LB Flour
- Package UPC: 000-16000-19580
- Recalled Better if Used By Date: 27 March 2024 and 28 March 2024
Gold Medal Bleached All Purpose 2LB Flour
- Package UPC: 000-16000-10710
- Recalled Better if Used By Date: 27 March 2024 and 28 March 2024
Gold Medal Bleached All Purpose 5LB Flour
- Package UPC: 000-16000-10610
- Recalled Better if Used By Date: 27 March 2024 and 28 March 2024

Healthy persons infected with Salmonella Infantis, a bacteria, often experience nausea, diarrhea, fever and abdominal pains. The CDC estimates there are 1.2 million cases annually in the U.S. Typically, symptoms start within six hours to six days after infection and last four to seven days. Any consumers concerned about an illness should contact a physician.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/general-mills-recalls-four-gold-medal-unbleached-and-bleached-all-purpose-flour-varieties-dated

Rushdi Foods Issues a Voluntary Recall on One Lot of Their Mighty Sesame Organic Tahini 10.9 oz Squeeze Bottle

May 3, 2023

More Information

Rushdi Food Industries, an Israeli based manufacturer, is voluntarily recalling their Mighty Sesame 10.9 Oz Organic Tahini (Squeezable) with the specific expiration date of 9/25/23 due t0 potential Salmonella contamination. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (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 severs illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

This recall was initiated when the company received a notification by the FDA and the Ohio Department of Health of the potential presence of Salmonella in this specific lot. The company has received no reports of illness or injury to date. We immediately informed all Stores who had purchased this product within this lot code about this Recall and instructed them to remove any product which might be on their shelves.

Only packages bearing the following Lot Code/Best by date are being recalled at this time. All products other than the ones with the affected Best by Date mentioned in the table are ok to consume.

UPC Code: 858313006208
Description: Mighty Sesame 10.9 oz Organic Tahini (Squeezable)
Expiration Date: 9/25/2023

The recalled product was distributed to stores predominately located in the New York, New Jersey and Connecticut regions as well as some stores nationwide during the weeks of February 23rd, 2023 through March 5th, 2023. Based off of sales velocity, there is an extremely low chance that any of the affected product would still be available for retail. All products other than the ones with the affected Best by Date mentioned in the table are ok to consume.

Consumers who may have purchased this product are advised to discontinue use immediately and discard or return the product for credit or refund. If a consumer experiences the symptoms listed above and believes they may have been exposed to Salmonella, they are urged to report to a medical provider.

Consumers who have questions may contact us at Customercare@kayco.com or by phone at 718-369-4600 Monday through Friday 9 AM to 5PM Eastern Time.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/rushdi-foods-issues-voluntary-recall-one-lot-their-mighty-sesame-organic-tahini-109-oz-squeeze-0

General Mills Recalls Four Gold Medal Unbleached and Bleached All Purpose Flour Varieties Dated March 27, 2024 and March 28, 2024

April 28, 2023

More Information

General Mills today announced a voluntary national recall of two-, five- and 10-pound bags of its Gold Medal Unbleached and Bleached All Purpose Flour with a “better if used by” date of March 27, 2024, and March 28, 2024. The recall is being issued for the potential presence of Salmonella Infantis,which was discovered during sampling of the five-pound bag product.

This recall affects two date codes of Gold Medal Unbleached All Purpose Flour in the five- and ten pound bags and two date codes of Gold Medal Bleached All Purpose Flour in the two- and five-pound bags. All other types of Gold Medal Flour are not affected by this recall.

Consumers are asked to check their pantries and dispose of the product affected by this recall. Consumers who have had to discard products covered by this recall may contact General Mills Consumer Relations at 1-800-230-8103.

Guidance from the Food and Drug Administration(FDA) and the Centers for Disease Control(CDC) warn that consumers should refrain from consuming any raw products made with flour. Salmonella Infantisis killed by heat through baking, frying, sautéing or boiling products made with flour. All surfaces, hands and utensils should be properly cleaned after contact with flour or dough.

This voluntary recall includes the following code dates currently in stores or consumers’ pantries:

Gold Medal Unbleached All Purpose 5LB Flour
- 000-16000-19610
Gold Medal Unbleached All Purpose 10LB Flour
- 000-16000-19580
Gold Medal Bleached All Purpose 2LB Flour
- 000-16000-10710
Gold Medal Bleached All Purpose 5LB Flour
- 000-16000-10610

Dakota Style Foods, Inc. Issues EXPANDED Allergy Alert on Undeclared Milk in Pretzels

April 22, 2023

More Information

Dakota Style Foods, Inc. is expanding the recall of the braided pretzels to include the following products 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 these products.

Pretzels were distributed through retail stores in all lower 48 states and Alaska.

Best by Dates and Lot Codes can be located on the back of the package.

No illnesses have been reported to date.

The expanded recall was initiated after further testing discovered additional products containing milk were distributed in packaging that did not reveal the presence of milk.

Consumers who have purchased these pretzels are urged not to consume them and to return the product to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-446-2779, Monday through Friday, 8:00am-5:00pm, CST.

Link to Initial Press Release

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dakota-style-foods-inc-issues-expanded-allergy-alert-undeclared-milk-pretzels?utm_medium=email&utm_source=govdelivery

Weinstein Wholesale Meats, Inc. Recalls Raw Ground Beef Burger Products Due to Possible Foreign Matter Contamination

April 21, 2023

More Information

Weinstein Wholesale Meats, Inc., a Forest Park, Ill. establishment, is recalling approximately 2,122 pounds of raw ground beef burger products that may be contaminated with extraneous materials, specifically pieces of white neoprene, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today.

The raw ground beef burger patties were produced on March 14, 2023. The following products are subject to recall [view labels]:

10.7-oz. vacuum-sealed packages containing two pieces of "100% Grass Fed & Finished Beef Burger Patties 85% Lean/15% Fat" and with "Use/Freeze By 4/11/23" on the package label.

The products subject to recall bear establishment number "Est. 6987" inside the USDA mark of inspection. These items were shipped to an online distributor, which sold the product to customers nationwide.

The problem was discovered after the establishment received multiple consumer complaints reporting consumers found white "rubber-like" material in the ground beef patty products during preparation.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

FSIS is concerned that some product may be in consumers' refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. 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 Nicole Schumacher, Chief Marketing Officer, Pre Brands LLC, at 844-773-3663 or reachus@eatpre.com. Members of the media with questions can contact Paul Esposito, Chief Operating Officer, Weinstein Wholesale Meats Inc., at 630-390-9138 or media@weinsteinmeats.com.

https://www.fsis.usda.gov/recalls-alerts/weinstein-wholesale-meats-inc--recalls-raw-ground-beef-burger-products-due-possible

Washington Crab Recalls Blue Crab Dip 8 oz, Cocktail Sauce 8 oz, Cole Slaw 8 oz and 16 oz & Crabcake 2, 6 & 12 Count Packages Due to Undeclared Milk, Egg, Wheat, Fish & Soy Allergens

April 21, 2023

More Information

Product	Size	Use By Dates	Missing Allergen
Blue Crab Dip	8 oz	10/24/2022 to 4/24/2023	Milk
Cocktail Sauce	8 oz	10/24/22 to 5/24/2023	Fish & Soy
Cole Slaw	8 oz & 16 oz	10/21/2022 to 4/21/2023	Egg & Soy
Crabcake	2, 6 & 12 count	10/13/2022 to 4/13/2023	Egg, Wheat & Soy

The products were distributed between Oct 13, 2022 to April 13, 2023. The Blue Crab Dip, Cocktail Sauce and Cole Slaw were packaged in clear plastic cups and Crabcakes on plastic trays and sold primarily to distributors, restaurants and company retail outlet located in the states of North Carolina & South Carolina.

Consumers who have purchased these products are urged to return them to the place of purchase for a full refund or they may discard the product. Consumers with questions may contact Michael Taylor at 252-946-5796 between hours of 8 AM to 6 PM EST Monday thru Friday EST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/washington-crab-recalls-blue-crab-dip-8-oz-cocktail-sauce-8-oz-cole-slaw-8-oz-and-16-oz-crabcake-2-6?utm_medium=email&utm_source=govdelivery

Wellness Natural USA Inc. EXPANDS Allergy Alert on Undeclared Cashews in SimplyProtein® Peanut Butter Chocolate Crispy Bars

April 12, 2023

More Information: Wellness Natural USA Inc. of Wilmington, DE is expanding their voluntary recall of its SimplyProtein® Peanut Butter Chocolate Crispy Bar, which is sold in a 15-count variety pack that contains two other flavors, because it may contain undeclared cashews. The initial recall which included a single lot has been expanded to include all lots within expiration, the Best Before dates are indicated below. 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 products were only distributed in Costco stores nationwide in the United States.

The product comes in a 15-count variety pack which includes 5 Peanut Butter Chocolate Crispy Bars. The product is marked with a Best Before date and Lot number on the bar wrapper (UPC 6 86207 00914 7) and on the outside carton (UPC 6 86207 80906 8). The photographs below indicate the location of Best Before date markings. Any product with the Best Before date between 11 APR 2023 and 14 MAR 2024 is included in this expanded recall.

The recall was voluntarily initiated due to a consumer complaint, which is the only reported reaction to date. It was determined the product may potentially contain undeclared cashew. The expansion comes following a decision by Wellness Natural USA Inc. to exercise an abundance of caution while the root cause of the contamination continues to be investigated.

Costco stores in the United States who are in possession of the product are urged to stop sales and distribution immediately, contain and isolate the affected products, and contact Wellness Natural USA Inc. for verification and disposal instructions. Consumers who have purchased the impacted products and have a sensitivity to cashew should not consume the product and return them to Costco for a full refund.

This product and the two other flavors in the carton, which declare cashew as an allergen, are safe to consume for people who do not have a sensitivity to cashew.

Any questions or concerns should be directed to contact@wellnessnaturalinc.com between the hours of 9:00 – 5:00 EST, Monday thru Friday.

Original Press Release

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/wellness-natural-usa-inc-expands-allergy-alert-undeclared-cashews-simplyproteinr-peanut-butter

Fresh Express Incorporated Announces Precautionary Recall of Expired Fresh Salad Kits Due to Potential Health Risk

April 7, 2023

More Information

Fresh Express Incorporated is voluntarily recalling a limited quantity of three varieties of already-expired branded and private label salad kit products produced at the company’s Morrow, Georgia facility out of an abundance of caution due to a possible health risk from Listeria monocytogenes. The recalled products are no longer available for sale and no illnesses have been reported to date.

Listeria monocytogenes can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. Consumers with these symptoms should consult their health care provider.

The recall was initiated when it was learned a random sample test of a single salad kit with a Use-By Date of March 31, 2023 collected by the Georgia Department of Agriculture yielded a positive result for the Listeria pathogen.

Recalled salad items all carry Product Code GO75 and Use-By Dates of March 31 or April 2, 2023 located on the front of the package. They were distributed through retailers in the states of Florida, Georgia, North Carolina, South Carolina and Virginia. Retailers have been instructed to ensure the recalled products are removed from all inventories. Consumers who might still have the recalled products in their refrigerators should discard and not consume them.

A listing of products subject to this recall are summarized at the end of this announcement.

To obtain a refund or for more information, consumers may call the Fresh Express Consumer Response Center at (800) 242-5472 between the hours of 8 a.m. to 7 p.m. Eastern Time. Refunds are also available where purchased.

Brand	Product	Ounce	UPC Codes	Product Code	Use-By Date	Distribution States
Fresh Express	Caesar Chopped Kit	9.4	00071279309194	G075	4/2/2023	FL, GA, NC, SC
Fresh Express	Chopped Kit Chipotle Cheddar	11.3	00071279306049	G075	4/2/2023	FL, GA, NC, SC, VA
Publix	Makoto Honey Ginger Salad Kit	8.75	00071279309194	G075	3/31/2023	FL, GA, NC

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresh-express-incorporated-announces-precautionary-recall-expired-fresh-salad-kits-due-potential

Seven Seas International USA, LLC is Voluntarily Recalling Biltmore Smoked Sockeye Salmon Because of Possible Health Risk

March 31, 2023

More Information

Sold at Publix Supermarkets only

Seven Seas International USA, LLC of St. Petersburg, Florida is voluntarily recalling 295 cases of Biltmore Smoked Sockeye Salmon with production lot R4058 because Listeria monocytogenes may be present in some product. The issue was discovered through routine regulatory testing conducted by the Florida Department of Agriculture and Consumer Services. Consumers who have purchased this product with this lot code are being advised not to consume it and return it to the store where it was originally purchased for a full refund. Listeria monocytogenes can cause serious and sometimes fatal infections, especially in preschool age children, older adults, or people who are immune compromised. Additionally, it can cause miscarriages and stillbirths in pregnant women. Only packages sold prior to 14th March 2023 which have a lot code R4058 printed on the clear plastic film that protects the product are affected by this recall, please check for this code, no other production codes are affected by this recall.

Customers who have additional questions or concerns may contact Seven Seas International USA, LLC at 1(888) 627-5668 or visit their website at www.7siusa.com.

Information regarding Biltmore Salmon products sold at Publix affected by this recall:

Product Name: Biltmore Smoked Sockeye Salmon
GTIN #: 007-36211-88774
Lot Code/Best By Date: R4058/April 14 2023

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/seven-seas-international-usa-llc-voluntarily-recalling-biltmore-smoked-sockeye-salmon-because?utm_medium=email&utm_source=govdelivery

Salento Organics Issues Allergy Alert on Undeclared Milk in Dark Chocolate Fruit and Peanut Bites

March 29, 2023

More Information

Salento Organics of West Palm Beach, Florida is recalling its 4 ounce packages of Dark Chocolate Pitaya Bites, Dark Chocolate Goldenberry Bites, Dark Chocolate Mango Bites, Dark Chocolate Banana Bites, Dark Chocolate Pineapple Bites and Dark Chocolate Peanut Bites because they may contain undeclared milk.

People who have allergies to milk run the risk of serious or life-threatening allergic reaction if they consume these products.
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The recalled Salento Organics products were distributed nationwide in retail stores and through mail orders.

The products recalled are:

Brand	Product	UPC	Lot	Best By
Salento Organics	Dark Chocolate Pitaya Bites	8-60006-27410-0	032214	2/1/2024
Salento Organics	Dark Chocolate Pitaya Bites	8-60006-27410-0	042214	2/1/2024
Salento Organics	Dark Chocolate Goldenberry Bites	8-60006-27411-4	032212	2/1/2024
Salento Organics	Dark Chocolate Goldenberry Bites	8-60006-27411-4	042212	2/1/2024
Salento Organics	Dark Chocolate Mango Bites	8-60006-27412-2	032210	2/1/2024
Salento Organics	Dark Chocolate Mango Bites	8-60006-27412-2	042210	2/1/2024
Salento Organics	Dark Chocolate Mango Bites	8-60006-27412-2	072210	5/1/2024
Salento Organics	Dark Chocolate Mango Bites	8-60006-27412-2	112210	5/1/2024
Salento Organics	Dark Chocolate Mango Bites	8-60006-27412-2	>012310	1/1/2025
Salento Organics	Dark Chocolate Banana Bites	8-60006-27414-6	032213	2/1/2024
Salento Organics	Dark Chocolate Banana Bites	8-60006-27414-6	042213	2/1/2024
Salento Organics	Dark Chocolate Banana Bites	8-60006-27414-6	072213	5/1/2024
Salento Organics	Dark Chocolate Banana Bites	8-60006-27414-6	112213	5/1/2024
Salento Organics	Dark Chocolate Banana Bites	8-60006-27414-6	12313	1/1/2025
Salento Organics	Dark Chocolate Pineapple Bites	8-60006-27413-9	032211	2/1/2024
Salento Organics	Dark Chocolate Pineapple Bites	8-60006-27413-9	042211	2/1/2024
Salento Organics	Dark Chocolate Pineapple Bites	8-60006-27413-9	072211	5/1/2024
Salento Organics	Dark Chocolate Pineapple Bites	8-60006-27413-9	112211	5/1/2024
Salento Organics	Dark Chocolate Pineapple Bites	8-60006-27413-9	12311	1/1/2025
Salento Organics	Dark Chocolate Peanut Bites	8-60006-27415-3	032215	2/1/2024
Salento Organics	Dark Chocolate Peanut Bites	8-60006-27415-3	042215	2/1/2024
Salento Organics	Dark Chocolate Peanut Bites	8-60006-27415-3	072215	5/1/2024
Salento Organics	Dark Chocolate Peanut Bites	8-60006-27415-3	112215	5/1/2024
Salento Organics	Dark Chocolate Peanut Bites	8-60006-27415-3	12315	1/1/2025

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

The recall was initiated after it was discovered that the milk-containing product was distributed in packaging that did not reveal the presence of milk.

Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's production and packaging processes.

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

Consumers who have purchased 4 ounce packages of Dark Chocolate Fruit and Peanut Bites, listed above are urged to return them to the place of purchase for a full refund.

Consumers with questions may contact the company at hello@salentorganics.com or calling at 561-402-8232, operational hours 9am EST – 5pm EST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/salento-organics-issues-allergy-alert-undeclared-milk-dark-chocolate-fruit-and-peanut-bites

Jarman’s Midwest Cleaning Systems, Inc. Issues Voluntary Nationwide Recall of Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution and Isopropyl Alcohol Antiseptic 75% Topical Solution Hand Sanitizer Non-sterile Solution

March 28, 2023

More Information

Jarman’s Midwest Cleaning Systems, Inc. is voluntarily recalling all lots of Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution and Isopropyl Alcohol Antiseptic 75% Topical Solution Hand Sanitizer Non-sterile Solution to the consumer level. FDA testing found the presence of methanol.

Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache blurred vision, coma, seizures, permanent blindness, permanent damage to the central nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute are most at risk for methanol poisoning. To date, Jarman’s Midwest Cleaning System’s Inc. has not received any reports of adverse events related to these products.

Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution and Isopropyl Alcohol Antiseptic 75% Topical Solution Hand Sanitizer Non-sterile Solution are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. The products are packaged in 1-gallon clear or white plastic bottles. The product may have been purchased by the 1-gallon bottle, or by the case which contains 4 of the 1-gallon bottles per box.

Product information:

Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution
- Midwest Cleaning Solutions 404 Noid Rd, Canton SD 57013 800-288-0741
  - DOM: 24 MAR through 18 Dec 2020
  - NDC: None
  - Volume: 3.785 L
- Clean Pro Supply, LLC 1533 Lyell Ave, Rochester, NY 14606 585-623-5075
  - DOM: 24 MAR 2020 through 18 DEC 2020
  - NDC: 77518-200-01
  - Volume: 1 Gallon, 128 FL OZ, 3785 mL
Isopropyl Alcohol Antiseptic 75% Topical Solution Hand Sanitizer Non-sterile Solution
- Midwest Cleaning Solutions 404 Noid Rd, Canton SD 57013 800-288-0741
  - DOM: 24 MAR 2020 through 18 DEC 2020
  - NDC: 74663-002-01
  - Volume: 3.785 L

Jarman’s Midwest Cleaning System’s Inc. is notifying its distributors by voluntary recall letters and consumers via this press release. Consumers that have the recalled products Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution and Isopropyl Alcohol Antiseptic 75% Topical Solution Hand Sanitizer Non-sterile Solution should stop using and either dispose of it in accordance with local ordinances, or contact Jarman’s Midwest Cleaning Systems, Inc. for returns at 1-800-288-0741 Monday – Friday 8:30 am to 5 pm Central Time or recall@mwcleaningsolutions.com.

Consumers with questions regarding this recall can contact Jarman’s Midwest Cleaning System’s Inc. at recall@mwcleaningsolutions.com or 1-800-288-0741 Monday – Friday 8:30 am to 5 pm Central Time. Consumers should contact their healthcare provider if they have experienced any health concerns that may be related to using these products.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/jarmans-midwest-cleaning-systems-inc-issues-voluntary-nationwide-recall-alcohol-antiseptic-80?utm_medium=email&utm_source=govdelivery

Second Nature Brands Issues Allergy Alert on Undeclared Wheat in Gluten Free Reese’s Pieces Brownie Brittle

March 23, 2023

More Information: Second Nature Brands of Madison Heights, MI, is recalling its 4-ounce packages of Gluten Free Reese’s Pieces Brownie Brittle because they may contain undeclared wheat.

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.

The recalled Gluten Free Reese’s Pieces Brownie Brittle were distributed nationwide in retail stores and through online orders.

The product comes in a 4-ounce pouch UPC 711747011562 marked with lot codes SG 1054 15/NOV/2023 1S and SG 1054 15/NOV/2023 2S on the backside of pouch.

One illness has been reported to date in connection with this problem, to date.

The recall was initiated after it was discovered that the gluten-containing product was distributed in packaging that did not reveal the presence of wheat. Subsequent investigation indicates the problem was caused by cross-contamination at a co-manufacturer, resulting in undeclared wheat in the product.

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

Consumers who have purchased 4-ounce packages of Gluten Free Reese’s Pieces Brownie Brittle with lot codes SG 1054 15/NOV/2023 1S and SG 1054 15/NOV/2023 2S should not consume the product and should contact Brownie Brittle for a full refund.

Consumers may contact the company by calling at (800) 651-7263 Monday-Friday from 8:30AM - 5:00PM EST or via email at recall@browniebrittle.com Second Nature Brands is conducting this recall with the full knowledge and cooperation of the U.S. Food and Drug Administration.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/second-nature-brands-issues-allergy-alert-undeclared-wheat-gluten-free-reeses-pieces-brownie-brittle?utm_medium=email&utm_source=govdelivery

Perrigo Announces Voluntary Recall of Limited Quantity of Gerber® Good Start® SootheProTM Powdered Infant Formula

March 17, 2023

More Information

Perrigo Company plc is issuing a voluntary recall of certain lots of Gerber® Good Start® SootheProTM Powdered Infant Formula in the U.S., that were manufactured at the Company’s Gateway Eau Claire, Wisconsin manufacturing facility from January 02, 2023 to January 18, 2023. This product is being recalled out of an abundance of caution due to the potential presence of Cronobacter sakazakii.

Importantly, no distributed product has tested positive for the presence of this bacteria, no adverse events have been reported and no other products manufactured at this facility or any other of Perrigo’s facilities are affected by this recall.

Cronobacter sakazakii is a bacteria commonly found in the environment. In most people it causes no symptoms but in some, particularly premature infants, infants under 2 months of age or infants with weakened immune systems fever, poor feeding, excessive crying or low energy as well as other serious symptoms can occur.|

This product is sold at retailers across the U.S. Consumers who purchased the product after March 5, 2023 should look for the following Lot Codes and “use by” dates, which can be found on the bottom of the package. No other lot codes are impacted by this recall. Any consumers who purchased product with matching codes should discontinue use and dispose of the product.

Gerber® Good Start® SootheProTM 12.4 oz:

300357651Z – USE BY 04JUL2024
300457651Z – USE BY 05JUL2024
300557651Z – USE BY 06JUL2024
300557652Z – USE BY 06JUL2024
300757651Z – USE BY 08JUL2024
300857651Z – USE BY 09JUL2024
301057651Z – USE BY 11JUL2024
301057652Z – USE BY 11JUL2024
301157651Z – USE BY 12JUL2024

Gerber® Good Start® SootheProTM 30.6 oz:

301357652Z – USE BY 14JUL2024
301457652Z – USE BY 15JUL2024
301557651Z – USE BY 16JUL2024

Gerber Good® Start® SootheProTM 19.4 oz:

301557652Z – USE BY 16JUL2024I

Consumers can request refunds for impacted products and find more information about Gerber® Good Start® by contacting the Gerber Parent Resource Center on behalf of Perrigo at 1-800-777-7690 anytime 24/7. Consumers with any health-related questions should contact their healthcare provider.

This recall is being conducted in consultation with the U.S. Food and Drug Administration (FDA).

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/perrigo-announces-voluntary-recall-limited-quantity-gerberr-good-startr-sootheprotm-powdered-infant?utm_medium=email&utm_source=govdelivery

Regional Recall: Clio Snacks Voluntarily Recalls Strawberry Granola & Greek Yogurt Parfait Bars from Select Walmart Stores Because of Possible Health Risk

March 15, 2023

More Information: Clio Snacks of Piscataway, N.J. is voluntarily recalling 581 cases of its Strawberry Granola & Greek Yogurt Parfait Bar due to potential contamination 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 to select Walmart stores between 3/5/2023 and 3/8/2023.

The impacted product comes in a single-serving box with UPC Code 854021008152, Lot Number 048C2023 and an expiration date of 4/30/2023 stamped on the side of the box.

Strawberry Granola & Greek Yogurt Parfait Bar is the only product impacted. No other products are being recalled. No illnesses have been reported to date.

This potential limited exposure was found at a third-party manufacturer’s facility where Parfait Bars are produced. The third-party manufacturer does not manufacture any other Clio products. Clio does not manufacture Parfait bars at its own facility.

The recall was the result of a routine testing program by the company which revealed that affected Strawberry Parfait product produced by Clio’s contract manufacturer may contain Listeria monocytogenes. The third-party manufacturer has ceased production and Clio has ceased distribution of the affected product while the FDA and the company continue their investigation into what caused the problem.

Consumers who have purchased Clio Strawberry Granola & Yogurt Parfait bar with an expiration date of 4/30/2023 should not consume the product and are urged to return it to the place of purchase for a full refund or to destroy the recalled product.

Consumers with questions may contact the company at 1-908-505-2546 (Monday – Friday, 9-5pm EST).

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/regional-recall-clio-snacks-voluntarily-recalls-strawberry-granola-greek-yogurt-parfait-bars-select

Nestlé Purina Petcare Company EXPANDS Voluntary Recall of Purina Pro Plan Veterinary Diets El Elemental Dry Dog Food in the U.S. Due to Potentially Elevated Vitamin D

March 10, 2023

More Information

Nestlé Purina PetCare Company is expanding its voluntary recall of Purina Pro Plan Veterinary Diets EL Elemental (PPVD EL) prescription dry dog food due to a supplier error resulting in potentially elevated levels of vitamin D in two additional product lots, which precede the production dates of the previously recalled lots. The original announcement was made on February 8, 2023. No other Purina pet care products are affected.

The expansion comes following an investigation prompted by Purina that uncovered new information about a production error from a U.S. supplier that was made only to this specific formula and resulted in potentially elevated levels of vitamin D.

Vitamin D is an essential nutrient for dogs; however, ingestion of elevated levels can lead to health issues depending on the level of vitamin D and the length of exposure. Vitamin D toxicity may include vomiting, loss of appetite, increased thirst, increased urination, and excessive drooling to renal (kidney) dysfunction.

A list of the additional impacted product is below. Bags of PPVD EL with the UPC Code and Production Code below should be immediately discarded.

Product

UPC Code

Production Code (*First 8 Characters equal to)

Purina Pro Plan Veterinary Diets EL Elemental (PPVD EL)
8 lb and 20 lb bags

38100 19190 – 8 lb
38100 19192 – 20 lb

2213 1082 (NEW)
2214 1082 (NEW)

The affected dry dog food was distributed throughout the United States by prescription only through veterinary clinics, Purina Vet Direct, Purina for Professionals, and other select retailers with the ability to validate a prescription.

Pet owners who purchased bags of the product listed above are asked to immediately stop feeding and throw it away in a container where no other animals, including wildlife, can get to it. If signs such as weight loss, excessive drooling, vomiting, loss of appetite or increased thirst or urination have occurred in their dog while eating this diet, pet owners should contact their veterinarian.

Veterinary and other retail partners should remove and destroy the affected product from their inventory.

Please contact our team directly Monday - Saturday, 8am - 5pm CST at 1-800-345-5678 or via email at https://www.purina.com/contact-us for questions or assistance in getting a refund.

Original Recall

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nestle-purina-petcare-company-expands-voluntary-recall-purina-pro-plan-veterinary-diets-el-elemental

Russell Stover Chocolates Issues Allergy Alert on Undeclared Pecan in Sugar Free Peanut Butter Cups

February 28, 2023

More Information: Russell Stover Chocolates of Kansas City, Missouri, is voluntarily recalling two (2) Best Before Dates of its Sugar Free Peanut Butter Cups in 2.4 oz packaging due to the potential for undeclared pecans. The recalled Sugar Free Peanut Butter Cups may contain Sugar Free Pecan Delights. Pecans are not declared on the label. People who have an allergy or severe sensitivity to pecans run the risk a serious or life-threatening allergic reaction if they consume these products.

The recalled Sugar Free Peanut Butter Cups were distributed nationwide to wholesale and retail stores.

The recalled Sugar Free Peanut Butter Cups are packaged in a 2.4 oz plastic bag, and they are labeled with Best Before dates of 01MAY23 and 01JUN23 and UPC of 077260096937 with Lot code(s): K0521, K0321, K0421, L2122, L2221, L2321. The lot code and best before date can be found on the back of the product packaging, below the UPC.

The recall was initiated following consumer contacts regarding the wrong product inside the outer packaging for Sugar Free Peanut Butter Cups product. Russell Stover has received no reports of any illness or allergic reactions related to this issue to date.

An error by the firm’s 3rd party co-packing company resulted in individually-wrapped Sugar Free Pecan Delight products being placed in the outer packaging for Sugar Free Peanut Butter Cups. The inner packaging correctly identifies the products as Sugar Free Pecan Delights and the physical Sugar Free Pecan Delight product appears distinct from the Sugar Free Peanut Butter Cup product.

Consumers who may have purchased this product may contact Russell Stover Chocolates directly for a voucher or replacement product. If you have any questions, please contact Russell Stover Chocolates on our website using the Contact Us Form at https://www.russellstover.com/contact-us, or by email at consumerservices@russellstover.com or at 1-800-477-8683 operating hours Monday – Friday 8AM-5PM CST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/russell-stover-chocolates-issues-allergy-alert-undeclared-pecan-sugar-free-peanut-butter-cups

nanoMaterials Discovery Corporation Issues Voluntary Nationwide Recall of its Alcohol Antiseptic 80% Alcohol Solution

February 21, 2023

More Information: nanoMaterials Discovery Corporation is voluntarily recalling all lots of its Alcohol Antiseptic 80% Alcohol Solution branded as “Snowy Range Blue” in four fluid ounce spray dispenser packaging to the consumer level. Certain batches of the company’s Alcohol Antiseptic 80% Alcohol Solution may exceed FDA limits for methanol.

Risk Statement: The affected Alcohol Antiseptic 80% Alcohol Solution with methanol concentrations that exceed FDA limits potentially could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute are most at risk. nanoMaterials Discovery Corporation has not received any reports of adverse events related to this recall.

The product is used as a hand sanitizer to help reduce bacteria that potentially can cause disease. The product is for use when soap and water are not available. The affected Alcohol Antiseptic 80% Alcohol Solution is packaged in four fluid ounce spray dispenser bottles bearing the code NDC 75288-100-04. The product can be identified by the four fluid ounce spray dispenser bottle packaging and the product labeling pictured below. The affected Alcohol Antiseptic 80% Alcohol Solution was sold nationwide to distributors. Sales of this product were discontinued in Q4 2021.

nanoMaterials Discovery Corporation is notifying its distributors by mail and is arranging for return or disposal of all recalled products. Consumers/distributors/retailers that have Alcohol Antiseptic 80% Alcohol Solution branded as “Snowy Range Blue”, which is being recalled, should stop using and return to place of purchase or discard.

Consumers with questions regarding this recall can contact nanoMaterials Discovery Corporation at anesepticrecall@gmail.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nanomaterials-discovery-corporation-issues-voluntary-nationwide-recall-its-alcohol-antiseptic-80?utm_medium=email&utm_source=govdelivery

Colgate-Palmolive Recalls Fabuloso Multi-Purpose Cleaners Due to Risk of Exposure to Bacteria

February 8, 2023

More Information

Name of Product:
Fabuloso Multi-Purpose Cleaners
Hazard:
The recalled products can contain Pseudomonas species bacteria, including Pseudomonas aeruginosa and Pseudomonas fluorescens, which are environmental organisms found widely in soil and water. People with weakened immune systems, external medical devices, or underlying lung conditions who are exposed to the bacteria face a risk of serious infection that may require medical treatment. The bacteria can enter the body if inhaled, through the eyes, or through a break in the skin. People with healthy immune systems are usually not affected by the bacteria.
Remedy:
Refund/Replace

This recall involves certain Fabuloso Multi-Purpose Cleaners, which is a multi-purpose cleaner that can be used to clean most residential hard surfaces. The first 8 digits of the lot code of the recalled products are 2348US78 through 2365US78 and 3001US78 through 3023US78. A list of the UPC and lot codes of the recalled products can be found at www.Fabulosorecall.com. For a complete list of products, visit www.Fabulosorecall.com. The lot code is located on the back of the bottle above the label either directly above or towards the top of the bottle. No Fabuloso Antibacterial variants or other Fabuloso products are impacted by this recall. The following Fabuloso Multi-Purpose Cleaners are included in this recall.

Lavender Scent
- Fabuloso Original Multi-Purpose Cleaner, Lavender Scent, 22 FL OZ
- Fabuloso Multi-Purpose Cleaner 2X Concentrated Formula, Lavender Scent,
- 56 FL OZ, 128 FL OZ, 169 FL OZ
- Fabuloso Multi-Purpose Cleaner, Lavender Scent, 210 FL OZ
- Fabuloso Professional All-Purpose Cleaner & Degreaser, Lavender Scent, 1 GALLON
Refreshing Lemon Scent
- Fabuloso Original Multi-Purpose Cleaner, Refreshing Lemon Scent, 22 FL OZ
- Fabuloso Multi-Purpose Cleaner 2X Concentrated Formula, Refreshing Lemon Scent,
- 33.8 FL OZ, 56 FL OZ, 128 FL OZ and 169 FL OZ
Passion of Fruits Scent
- Fabuloso Multi-Purpose Cleaner 2X Concentrated Formula, Passion of Fruits Scent,
- 33.8 FL OZ, 56 FL OZ, 128 FL OZ and 169 FL OZ
Spring Fresh Scent
- Fabuloso Multi-Purpose Cleaner Bleach Alternative 2X Concentrated Formula, Spring Fresh Scent, 56 FL OZ
Ocean Scent
- Fabuloso Professional All-Purpose Cleaner & Degreaser, Ocean Scent, 1 GALLON

Remedy:
Consumers should immediately stop using the recalled Fabuloso Multi-Purpose Cleaner products and contact Colgate-Palmolive Company for a full refund or a free replacement product. To receive a refund or replacement, consumers should take a picture of the product’s UPC and lot code and dispose of the product in its container with household trash. The consumer recall form can be found on www.fabulosorecall.com. Do not empty the product prior to disposal.
Incidents/Injuries:
None reported.
Sold At:
Online at Amazon.com and other websites and at Dollar General, Family Dollar, The Home Depot, Sam’s Club, Walmart, and other major retailers nationwide from December 2022 through January 2023 for between $1 and $11.

https://www.cpsc.gov/Recalls/2023/Colgate-Palmolive-Recalls-Fabuloso-Multi-Purpose-Cleaners-Due-to-Risk-of-Exposure-to-Bacteria

Reckitt Recalls Two Batches of Prosobee 12.9 oz Simply Plant Based Infant Formula Because of Possible Health Risk

February 20, 2023

More Information: Product tested and confirmed negative for contaminants.

No reported adverse consumer reactions to date.

Reckitt, a producer of nutrition products, announced today that, out of an abundance of caution, it has chosen to voluntarily recall two (2) select batches of ProSobee 12.9 oz. Simply Plant-Based Infant Formula due to a possibility of cross-contamination with Cronobacter sakazakii. All product distributed went through extensive testing and tested negative for the bacteria.

ProSobee Simply Plant-Based Infant Formula in 12.9 oz containers was manufactured between August 2022 and September 2022. The products were distributed through retail stores nationwide in the U.S., Guam, and Puerto Rico. The batches in question can be identified by the number on the bottom of the can. Recalled product batches are ZL2HZF and ZL2HZZ both with a UPC Code of 300871214415 and a “Use By Date” of “1 Mar 2024.” The recall involves approximately 145,000 cans.

No other ProSobee Simply Plant-Based Infant Formula batches or other Reckitt products are impacted.

No illnesses or adverse events have been reported. If parents have any questions, they should consult with their pediatrician or contact us at 1-800-479-0551 24/7 or by email at consumer.relations@rb.com

We are committed to the highest level of quality and safety and it is for this reason that we have taken this extraordinary measure. The batches in question tested negative for Cronobacter and other bacteria and this is an isolated situation. After a thorough investigation, we have identified the root cause, which was linked to a material from a third party. We have taken all appropriate corrective actions, including no longer sourcing this material from the supplier.

The health and safety of infants is our highest priority. All of our products undergo rigorous and industry leading quality tests and checks to ensure that they meet or exceed all standards set by regulatory bodies, including the World Health Organization and the U.S. Food and Drug Administration. It is for this reason that we have the highest level of confidence in the safety and quality of every infant formula we make.

What Consumers Should Do if They Purchased This Product

Consumers who purchased ProSobee Simply Plant-Based Infant Formula should check the bottom of the can to identify whether the batch number is affected. Product with batch codes ZLZHZF and ZLZHZZ both with a UPC Code of 300871214415 and a “Use By Date” of “1 Mar 2024” should be disposed of or returned to the place of purchase for a total refund. You can also contact us at 800-479-0551 or by email at consumer.relations@rb.com and we will help verify if this product was impacted.

If you have any concerns, contact your health care provider. For more information please visit us at www.enfamil.com

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/reckitt-recalls-two-batches-prosobee-129-oz-simply-plant-based-infant-formula-because-possible

Silvestri Sweets Issues Voluntary Allergy Alert on Undeclared Pecan in Milk Chocolate Caramels

February 16, 2023

More Information

Silvestri Sweets Inc. of Geneva, IL is voluntarily recalling its 8-ounce bags of Favorite Day branded Valentine’s Milk Chocolate Covered Caramels with Nonpareils because they may contain an undeclared tree nut. People who have allergies to tree nuts {chestnuts, brazil nuts, walnuts, hazelnuts, pecans, pine nuts, cashews} run the risk of serious or life-threatening allergic reaction if they consume these products.

The recalled items were distributed nationwide through Target retail stores.

The products are packed in 8 oz. Favorite Day branded stand up pouch bags with the lot # 33822 and best by date on 07 DEC 2023, which are printed on the back of the bag underneath the UPC barcode.

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

The recall was initiated after it was discovered that possible tree nut inclusions were distributed in packaging and/or product that did not reveal the presence of tree nuts. Subsequent investigation indicates the problem may have been caused by a temporary breakdown in the company’s production and packaging process.

Consumers who have purchased 8-ounce bags of the Favorite Day Valentine’s Milk Chocolate Caramels with nonpareils are urged to call Target Guest Relations at 1-800-440-0680 (24/7) for a refund.

Consumers with questions may contact Silvestri Sweets at 1-630-232-2500 - M-F 8:30am-4:30pm CST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/silvestri-sweets-issues-voluntary-allergy-alert-undeclared-pecan-milk-chocolate-caramels?utm_medium=email&utm_source=govdelivery

Wismettac Asian Foods Issues Allergy Alert on Undeclared Spice Seasoning

February 14, 2023

More Information: Wismettac Asian Foods, Inc., Santa Fe Springs, CA is recalling 10.58 oz packages of Shirakiku brand Spice Seasoning products (Spice Ichimi Togarashi 300g and Spice Shichimi Togarashi 300g). The product package of Ichimi spice seasoning contains Shichimi spice seasoning contents (incorrect package) causing the undeclared allergen of sesame seeds. The outer carton of “Ichimi” and “Shichimi” may possibly contains inner packages of “Ichimi”, and the inner packages contain “Shichimi” contents.

People who have an allergy or severe sensitivity to seasame run the risk of serious or life-threatening allergic reaction if they consume these products.

The product was distributed in AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, Il, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, VA, WA, WI, WV mainly through restaurants and some through retail stores.

The product comes in a 10.58 oz, clear plastic bag. The affected lot code specified on the package is 12262023, distributed between June 27, 2022 and February 8, 2023. The UPC for the product is 074410341169

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

The recall was initiated after it was discovered that the product containing sesame was distributed in packaging that did not reveal the presence of sesame. Subsequent investigation indicates the problem was caused by a human error during the packing process.

The distribution of the product has been ceased until the company is certain that the problem has been corrected.

Consumers who have purchased the product are urged to return them to the place of purchase for a full refund.

Consumers with questions may contact the company at recall@wismettacusa.com.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/wismettac-asian-foods-issues-allergy-alert-undeclared-spice-seasoning?utm_medium=email&utm_source=govdelivery

Fresh Ideation Food Group LLC Recalls Sandwiches and Other Products Because of Possible Health Risk

February 3, 2023

More Information: Fresh Ideation Food Group LLC of Baltimore, MD is recalling products sold from January 24, 2023, through January 30, 2023, because the products have the potential to be contaminated with Listeria monocytogenes an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

Products have been distributed in Connecticut, District of Columbia, Maryland, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, and Virginia. Recalled Products were sold in retail locations, vending machines, and during travel with transportation providers.

The products include sandwiches, salads, snacks, yogurt, wraps and related products. A listing of the relevant product information is provided at the bottom of this press release.

All recalled products have a Fresh Creative Cuisine label and/or identifier on the bottom of the label with the Fresh Creative Cuisine name and a fresh through or sell through date ranging from January 31, 2023 through February 6, 2023.

The recall was initiated after the company’s environmental samples tested positive for Listeria monocytogenes.

No illnesses have been reported to date.

Consumers who have purchased the products are urged to contact the company, Fresh Ideation Food Group LLC, at 855-969-3338, Monday through Friday, 8am to 4pm EST.

Review the link below for a complete list of recalled products.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresh-ideation-food-group-llc-recalls-sandwiches-and-other-products-because-possible-health-risk

Delight Foods USA LLC Recalls Ineligible Frozen Siluriformes Products Imported from India

February 3, 2023

More Information

Delight Foods USA LLC, a distributor and the Importer of Record located in Jersey City, N.J., and Delight Foods LLC, a distributor and the Importer of Record located in San Jose, Calif., is recalling approximately 2,961 pounds of imported frozen Siluriformes (catfish) products. The products were imported from India, a country ineligible to export Siluriformes products to the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The following raw, frozen products are subject to recall, regardless of the product date [view labels]:

908 gm (2 lb.) plastic packages containing “Seafood delight FRESH FROZEN CATFISH STEAK IF” frozen fish.

The products do not bear an establishment number nor a USDA mark of inspection. These items were shipped to retail locations nationwide.

The problem was discovered during routine FSIS surveillance activity of imported products. India is not eligible to export Siluriformes products to the United States.

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 the product may be in retailers’ or consumer’s 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 Joseph Parayil, Member, Delight Foods USA LLC & Delight Foods LLC, at info@dailydelight.com and 201-369-1199.

https://www.fsis.usda.gov/recalls-alerts/delight-foods-usa-llc-recalls-ineligible-frozen-siluriformes-products-imported-india

B&G Foods Issues Voluntary Allergy Alert for Undeclared Peanut in Three Cases of Back to Nature® Fudge Mint Cookies

February 1, 2023

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B&G Foods announced today it is voluntarily recalling three cases (18 individual boxes) of a single date code of 6.4 oz. Back to Nature Fudge Mint Cookies, with a “best by” date of OCT 02,2023, after being notified that an ingredient supplied by a third-party ingredient supplier was contaminated with peanut, an allergen not declared on the cookie box label. People who have an allergy or severe sensitivity to peanut run the risk of serious or life-threatening allergic reaction if they consume the cookies contained in the three recalled cases.

This recall affects only three cases of the following product, which may have been distributed in retail stores nationwide:

Back to Nature Fudge Mint Cookies | 8-19898-01102-5 | 6.4 oz. | OCT 2 2023 (The "best by" date 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 have been reported to date. This recall was initiated in cooperation with the FDA and the third-party co-packer that produces the cookies after it was discovered that an ingredient supplied by a third-party ingredient supplier was contaminated with peanut.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bg-foods-issues-voluntary-allergy-alert-undeclared-peanut-three-cases-back-naturer-fudge-mint?utm_medium=email&utm_source=govdelivery

FSIS Issues Public Health Alert for Ready-To-Eat Meat Snack Products Containing FDA-Regulated Wafers that Have Been Recalled Due to Misbranding and an Undeclared Allergen

February 1, 2023

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The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) meat snack products containing Food and Drug Administration (FDA) regulated chocolate wafers that have been recalled due to an undeclared allergen, specifically peanut residue. FSIS is issuing this public health alert to ensure that consumers are aware that this product should not be consumed.

The meat snack items were produced with the recalled chocolate wafers on various dates from January 2, 2023, through January 18, 2023. The following products are subject to the public health alert [view labels]:

2.71-oz. plastic tray packages containing “PRIVATE SELECTION SNACK BOARD SMOKED DRY CURED RED WINE SALAMI” with lot code 11110900408 and Best By dates of “APR 10 2023” and “APR 18 2023”.
3-oz. plastic tray packages containing “GREENFIELD NATURAL MEAT CO. SMOKED UNCURED PEPPERONI” with lot code 63100268821 and Best By date “APR 03 2023”.
2.9-oz. plastic tray packages containing “PRIVATE SELECTION SNACK BOARD SMOKED DRY CURED SPICY CALABRESE SALAMI” and lot code 11110605471 with Best By date of “APR 03 2023”and “APR 19 2023”.

The products subject to the public health alert bear establishment number “645” inside the Canadian mark of inspection. These items were shipped to retail locations nationwide.

The problem was discovered when the producing establishment was notified by their wafer supplier that the chocolate wafers are being recalled because they may contain peanut residue, a known allergen, which is not declared on the label. The Canadian Food Inspection Agency (CFIA) notified FSIS that the recalled wafers were used in products distributed to the United States.

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. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

Consumers with questions about the public health alert can contact Maple Leaf Foods Inc. at 1-877-526-4520. Members of the media who have questions can contact Maple Leaf Foods Inc. at media.hotline@mapleleaf.com.

https://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-ready-eat-meat-snack-products-containing-fda

Conagra Brands Recalls Canned Meat and Poultry Products Due to Possible Packaging Defect

January 31, 2023

More Information: Conagra Brands, Inc., a Fort Madison, Iowa establishment, is recalling approximately 2,581,816 pounds of canned meat and poultry products due to a packaging defect that may cause the products to become contaminated without showing any outward signs of contamination, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The meat and poultry products were produced between December 12, 2022, and January 13, 2023. The following products are subject to recall: [view spreadsheet] [view labels].

The products subject to recall bear establishment number “P4247” on the product cans. These items were shipped to retail locations nationwide.

The problem was discovered when the establishment notified FSIS after observing spoiled and/or leaking cans from multiple production dates at the establishment’s warehouse.

Subsequent investigation by the establishment determined that the cans subject to recall may have been damaged in a manner that is not readily apparent to consumers, which may allow foodborne pathogens to enter the cans.

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 on retail shelves or 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 recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution lists will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Members of the media with questions about the recall can contact Dan Hare, Senior Director of Communications, ConAgra Brands, at 312-549-5355 or daniel.hare@conagra.com. Consumers with questions about the recall can call 800-289-6014, Monday-Friday 9 a.m. to 5 p.m. CST or email consumer.care@conagra.com.

https://www.fsis.usda.gov/recalls-alerts/conagra-brands-recalls-canned-meat-and-poultry-products-due-possible-packaging

Daniele International LLC Recalls Ready-to-Eat Sausage Products Due to Possible Listeria Contamination

January 29, 2023

More Information

Daniele International LLC, a Mapleville, R.I., establishment, is recalling approximately 52,914 pounds of ready-to-eat (RTE) sausage products that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The RTE sausage products were produced on various dates from May 23, 2022, through November 25, 2022, and shipped to retail locations nationwide on various dates from December 23, 2022, through January 17, 2023. The following products are subject to recall [view labels]:

6-oz. plastic tray of “FREDERIK’S by Meijer SPANISH STYLE charcuterie sampler tray” with sell by date 4/15/23.
6-oz. plastic tray of “Boar’s Head CHARCUTUERIE TRIO” with sell by dates 4/13/23, 4/14/23, and 4/15/23.
7-oz. plastic tray of “COLAMECO’S PRIMO NATURALE GENOA UNCURED SALAMI” with sell by date 12/23/23.
7-oz. plastic tray of “COLAMECO’S PRIMO NATURALE BLACK PEPPER UNCURED SALAMI” with use by dates 12/22/23, 12/30/23, and 1/17/24.
1-lb. plastic tray of “DEL DUCA SOPRESSATA, COPPA & GENOA SALAMI” with sell by dates 4/13/23 and 4/14/23.
1-lb. plastic tray of “DEL DUCA CALABRESE, PROSCIUTTO & COPPA” with sell by date 5/6/23.
1-lb. plastic tray of “DEL DUCA GENOA SALAMI, UNCURED PEPPERONI & HARD SALAMI” with use by date 5/4/23.
12-oz. plastic tray of “Gourmet Selection SOPRESSATA, CAPOCOLLO, HARD SALAME” with sell by date 4/14/23.

The products subject to recall bear establishment number “EST. 54” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.

FSIS discovered the problem during routine inspection activities where Listeria monocytogenes was found on surfaces in which the product came into contact.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.

Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.

FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Media with questions regarding the recall can contact Chris Bowler, CEO, Daniele International LLC, at 202-288-3372 or Chris.Bowler@charcuterie.com. Consumers with questions regarding the recall can contact Dee Traynor, receptionist, Daniele International LLC, at 401-568-6228 or receptionist@charcuterie.com.

https://www.fsis.usda.gov/recalls-alerts/daniele-international-llc-recalls-ready-eat-sausage-products-due-possible-listeria

Garden of Light (dba Bakery On Main) Voluntarily Recalls Oat & Honey Organic Granola Due to Potential Almond Contamination

December 30, 2022

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Garden of Light (dba Bakery On Main is voluntarily recalling one lot of Organic Oat and Honey Granola for possible Tree nut (Almond)contamination. People who have an allergy or severe sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume this product.

Product is sold at retailers nationally under the brands:

Topco/Full circle Organic Oat & Honey Granola with UPC code of 036800420397
SEG stores under the “Naturally Better” Organic Oats & Honey Granola with UPC code of 07880201130.

The product was produced with a “Best Before Date” (BBD) of 10/10/23. The best before date and UPC code can be found on the back of the film package.

No other lot codes or products are impacted by this voluntary recall.

The company manufactured 14,304 pounds of product which was distributed by Total Granola in Topco and SEG retail stores throughout the United States. The product recall was voluntarily initiated after it was discovered that product potentially containing Almonds was distributed in packaging that did not reveal the presence of Almonds. No illnesses or injuries have been reported to date.

Customers with product with the 10/10/22 BBD in their possession should dispose of it immediately. If consumers have any questions, they can contact Garden of Light (dba as Bakery On Main) at info@bakeryonmain.com or 860-895-6622. Responses will be provided Monday- Friday 8:00 am – 5:00 pm EST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/garden-light-dba-bakery-main-voluntarily-recalls-oat-honey-organic-granola-due-potential-almond?utm_medium=email&utm_source=govdelivery

Alpha Foods Issues a Product Recall Due to Undeclared Milk in Meatless Burritos & Breakfast Sandwiches

December 21, 2022

More Information

Out of an abundance of caution, Miso Brothers, Inc. dba Alpha Foods, is voluntarily recalling its Meatless Breakfast Sandwiches and Burritos due to traces of undeclared milk (Casein - a milk protein), that may pose a health risk for those with milk allergies.

The Meatless Breakfast Sandwiches and Burritos were distributed nationally throughout retail stores and shipped directly to consumers who purchased our products online.

Alpha Foods Meatless Burritos and Breakfast Sandwiches with the following lot codes, located on the back of the product, are being voluntarily recalled:

Product Description

Lot Number

UPC

Expiration Date

Bac'n Scramble Breakfast Burrito

052822BSB

855099007948

5/28/2024

Bac'n Scramble Breakfast Burrito

062022BS

855099007948

6/20/2024

Meatless Sausage Breakfast Sandwich

092122MSS

810070350093

9/21/2024

Meatless Chorizo Breakfast Sandwich

062822SCS

810070350109

6/28/2024

Meatless Chorizo Breakfast Sandwich

070722SCS

810070350109

7/7/2024

Chik'n Fajita Burrito

031522CFB

855099007047

3/15/2024

Chik'n Fajita Burrito

041322CFB

855099007047

4/13/2024

Chik'n Fajita Burrito

P2-22109

855099007047

4/19/2024

Meatless Sausage Breakfast Burrito

081122MSB

855099007733

8/11/2024

Meatless Sausage Breakfast Burrito

101522MSS

855099007733

10/15/2024

Meatless Sausage Breakfast Burrito

110222MSB

855099007733

11/2/2024

Philly Burrito

072822PB

855099007023

7/28/2024

Philly Burrito

101822PB

855099007023

10/18/2024

Philly Burrito

P2-22266

855099007023

9/23/2024

Pizza Burrito

041422PB

855099007016

4/14/2024

Steakless Ranchero Burrito

022422SRB

855099007764

2/24/2024

To date, there have been no illnesses or allergic reactions as a result of this recall.

This recall was initiated after it was discovered that the products containing traces of undeclared milk (Casein - a milk protein) were distributed in retail stores and delivered directly to consumers who purchased our products online. Subsequent investigation indicates that the contamination is likely to have occurred during the production of our products.

Consumers who have purchased our products with the identified lot numbers above, should not consume the products. Return the product to the place of purchase for a replacement or full refund. Consumers with questions may contact Alpha Foods via email at customerservice@eatalphafoods.com.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/alpha-foods-issues-product-recall-due-undeclared-milk-meatless-burritos-breakfast-sandwiches

Meijer Announces Allergy Alert on Undeclared Almonds in True Goodness Oat-Based Plain Yogurt Alternative

December 22, 2022

More Information

Culture Fresh Foods is issuing a recall for True Goodness by Meijer Oat-Based Plain Yogurt Alternative 24 Oz due to an undeclared - almonds. People who have an allergy or severe sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume this product. The recall was initiated after discovering that tubs labeled as Oat-Based, actually contain Almond-Based product, which is not listed on the product label.

Product Description: The affected products are those with identifying attributes seen below.

Hazard: Undeclared allergen - Almonds.

Manufacturer: Culture Fresh Foods, Inc.

UPC Carried by Meijer:

UPC

UPC Description

Lot Code

7-13733-03918-5

TRUE GOODNESS OAT MILK YOGURT PLAIN 24 OZ

2002

What You Should Do: Consumers who have purchased this product should discontinue use immediately and return the product to the nearest Meijer store for a full refund.

Consumer Contact Information: Consumers with questions regarding this recall should contact Culture Fresh Foods, Inc. at 203-632-8433.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/meijer-announces-allergy-alert-undeclared-almonds-true-goodness-oat-based-plain-yogurt-alternative

Mountain View Packaging, LLC, Recalls Frozen Ready-To-Eat Crispy Chicken with Almonds Entrée Products Due to Misbranding and an Undeclared Allergen

December 15, 2022

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Mountain View Packaging, LLC, a Boise, Idaho establishment, is recalling approximately 6,013 pounds of frozen, ready-to-eat Crispy Chicken with Almonds entrée 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 shellfish (shrimp), a known allergen, which is not declared on the product label.

The frozen, ready-to-eat Crispy Chicken with Almonds entrée products were produced November 17, 2022. The following product is subject to recall [view labels]:

18.5 oz packages of “INNOVASIAN Crispy Chicken with Almonds ENTREE” with lot code 22321-1, UPC code 695119120499, and a best by date 05/24/2023.

The product subject to recall bears the USDA mark of inspection but does not bear the establishment number on the packaging. These items were shipped to retail locations nationwide.

The problem was discovered when the firm notified FSIS that they received a consumer complaint reporting shrimp in a product labeled as Crispy Chicken with Almonds entrée.

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’ or retailers’ freezers. Consumers who have purchased these products are urged not to consume them and retailers are urged not to sell them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution lists will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers with questions about the recall can contact the InnovAsian Cuisine hotline at 1-800-324-5140. Members of the media with questions about the recall can contact Sunshine Morrison, Radiance Communications, at sunshine@radiancecom.com.

https://www.fsis.usda.gov/recalls-alerts/mountain-view-packaging-llc-recalls-frozen-ready-eat-crispy-chicken-almonds-entree

Utopia Foods Recalls “Enoki Mushrooms” Because of Possible Health Risk

December 13, 2022

More Information: Utopia Foods Inc of Glendale, NY, is recalling its 200g packages of “Enoki Mushrooms”, imported from China and distributed nationwide in the US, 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 “Enoki Mushrooms” were distributed nationwide in produce wholesale companies.

The product comes in a 200g, clear and blue plastic package with brand name “Utopia” and barcode# 8928918610017 marked on the packaging.

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

The potential contamination was noted by a routine sampling conducted in the State of Missouri revealed the presence of Listeria monocytogenes in the 200g packages of “Enoki Mushrooms”.

The distribution of the product has been suspended while FDA and the company continue to investigate the source of the problem.

All Utopia branded Enoki Mushrooms imported from China and within expiry are effected by the recall. Consumers who have purchased the 200g packages of “Enoki Mushrooms” within expiry are urged to return them to the place of purchase for a refund.

Consumers with questions may contact the company at 718.389.8898 Monday-Friday EST 8AM-4PM.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/utopia-foods-recalls-enoki-mushrooms-because-possible-health-risk

Northern Food I/E Recalls “Sweetened Jujube” Due to Undeclared Sulfites

December 7, 2022

More Information: Northern Food I/E Inc. of Westbury, NY is recalling all lots and codes of its 8.3-ounce (235-gram) packages of “Lukai sweetened jujube” because they may contain undeclared sulfites. People who have a severe sensitivity to sulfites run the risk of serious or life-threatening reactions if they consume this product.

The recalled “Lukai sweetened jujube” was distributed nationwide. The product comes in an 8.3 ounce red and yellow plastic package. The product UPC code is 6921996166881.

No illnesses or adverse reactions involving this product have been reported to date.

The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed that the sulfite containing product was distributed in packages that did not reveal the presence of sulfites.

Consumers who have purchased 8.3-ounce packages of “Lukai sweetened jujube” are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 516-942-0146.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/northern-food-ie-recalls-sweetened-jujube-due-undeclared-sulfites

Cranberry Sweets & More Issues Allergy Alert On Undeclared Peanuts In “Mint Meltaways”

December 6, 2022

More Information: Cranberry Sweets & More of Coos Bay, Oregon is voluntarily recalling its 4 and 8 ounce packages of "Mint Meltaways" candies 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 Mint Meltaways were distributed to retail stores in Oregon and Washington and sold nationwide through mail orders since September 21, 2022 to date.

The affected product is packaged in clear cellophane bags, net wt. 4oz and 8 oz. and has no UPC. The front label is read “Mint Meltaways” and the back label is read “Heirloom Mint Meltaways”. The affected product is marked with lot #032123 on the bottom.

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

The recall was initiated after it was discovered that the Peanut Butter Meltaways product was mis-labeled as Heirloom Mint Meltaways and peanut was not declared on finished product label. The firm’s subsequent investigation indicates the problem was caused by a temporary breakdown in the company's packaging process. The process has been corrected and the company has instituted additional safety checks and corrective actions.

This recall is being made with the knowledge of the U.S. Food and Drug Administration and the Oregon Department of Agriculture.

Consumers with a peanut allergy who have purchased the affected “Mint Meltaways” are urged not to consume the product and dispose of it or return it to their place of purchase for a full refund. Consumers with questions may contact the company at 1-800-527-5748 between 9am and 5:30pm PST, Monday-Friday.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/cranberry-sweets-more-issues-allergy-alert-undeclared-peanuts-mint-meltaways?utm_medium=email&utm_source=govdelivery

Nestlé Purina PetCare Company Voluntarily Recalls a Limited Amount of Purina Pro Plan Veterinary Diets EN Gastroenteric Low Fat Wet Dog Food Due to Labeling Error

December 2, 2022

More Information

Out of an abundance of caution, Nestlé Purina PetCare Company is voluntarily recalling a limited amount of Purina Pro Plan Veterinary Diets EN Gastroenteric Low Fat (PPVD EN Low Fat) prescription wet dog food in 13.4 oz cans due to a labeling error. For a brief period on September 15, 2022, cans of a different complete and balanced adult dog food, Purina ONE True Instinct Tender Cuts In Gravy With Real Turkey & Venison wet dog food, were labeled as PPVD EN Low Fat in one of our factories. The mislabeled diet is safe to feed, but it is not the intended formula for dogs requiring a prescription PPVD EN Low Fat diet, who may have sensitivities to traditional diets or difficulty digesting fat.

We became aware of the issue after being contacted by several pet owners who observed the texture of food in their PPVD EN Low Fat cans was not the same as previous meals. The mislabeled product contains chunks in gravy, while the correct product looks more like a pate consistency.

While we have not received any reports to date of illness or injury to dogs fed this mislabeled product, we are conducting this voluntary recall as a precaution. The affected product was available by prescription only and distributed through veterinary clinics and other retailers with the ability to validate a prescription. We have asked our veterinary and other retail partners to remove the affected product. We also recommend that you discard any of the affected product you may have, and we will replace it as quickly as possible.

You can identify the mislabeled product by the UPC (38100 17599), production code (22581159 L4TR6) and “Best Before Sept 2024” date on the bottom of each PPVD EN Low Fat can.

No other Purina products are impacted by this voluntary recall. We apologize to pet owners for any concerns or inconvenience this situation has caused. We’re pet owners too, and we know how important the health and well-being of our pets is, which is what led us to make this decision. We are taking action to investigate and notify pet owners and veterinarians of the situation. At Purina, pets always come first.

Please reach out to our team with any questions at 1-800-579-7733, Monday-Saturday, 8am - 5pm CST or via email at https://www.purina.com/contact-us.

Voluntary Recall of Purina Pro Plan Veterinary Diets EN Gastroenteric Low Fat Wet Dog Food

UPC Code

Best By

Production Code (*First 13 characters equal to)

38100 17599 (single 13.4 oz can)

SEPT 2024

22581159 L4TR6

Adam’s Polishes, LLC Issues Voluntary Nationwide Recall of Hand Sanitizer Due to Potential Contamination With Methanol

November 7, 2022

More Information

Thornton, Colorado, Adam’s Polishes, LLC is voluntarily recalling lot 133475 of Adam’s Polishes Hand Sanitizer to the consumer level. FDA testing has found this lot to contain undeclared methanol. Adam’s Polishes is recalling 19 other lots in an abundance of caution.

Risk Statement: Persons who accidently ingest (drink) these products are at risk for methanol poisoning. Substantial methanol ingestion can result in coma, seizures, permanent blindness, permanent damage to the central nervous system, or death. To date, Adam’s Polishes has not received any reports of injury, illness, or other adverse events related to this recall.

This product is used as a hand sanitizer marketed to help decrease bacteria on the skin when soap and water are not available. Adam’s Polishes Hand Sanitizer is packaged in 4oz., 8oz. 16oz., and one gallon bottles. These bottles are spray bottles for the 4oz, 8oz and 16oz and jugs for the gallon bottles. Please visit https://adamspolishes.com/pages/hs-voluntary-recall, This is the Adam’s Polishes web site to check if your product’s lot number is included in this recall and, if so, how to request a credit. The hand sanitizer was distributed nationwide in the USA to internet customers between June 2020 and March 2022.

133470

133471

133472

133473

133474

133475

133476

133477

133478

133479

133480

133481

133482

133483

137731

137732

137733

137734

139322

143327

Adam’s Polishes is notifying its customers by email. Consumers who have any recalled Adam’s Polishes Hand Sanitizer products should immediately stop using the product and dispose of it in accordance with local regulations. Consumers can email Adam’s Polishes with a request for a credit at hs@adamspolishes.com. You will need to include a picture of the bottle including the lot number.

Consumers with questions regarding this recall can contact Adam’s Polishes at e-mail address hs@adamspolishes.com . Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.

Office hours and telephone number 9 am – 4pm mst 720-812-3460

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/adams-polishes-llc-issues-voluntary-nationwide-recall-hand-sanitizer-due-potential-contamination?utm_medium=email&utm_source=govdelivery

Nestlé USA Announces Voluntary Recall of Limited Quantity of Edible Chocolate Chip Cookie Dough Tubs from NESTLÉ® TOLL HOUSE® Due to Potential Presence of Foreign Material

November 3, 2022

More Information

Nestlé USA is initiating a voluntary recall of a limited quantity of Edible Chocolate Chip Cookie Dough tubs from NESTLÉ® TOLL HOUSE® due to the potential presence of soft plastic film.

This voluntary recall is isolated to three batches of Edible Chocolate Chip Cookie Dough tubs from NESTLÉ® TOLL HOUSE® that were produced August 1-3, 2022. These products were distributed to retailers nationwide.

This recall does not involve any other NESTLÉ® TOLL HOUSE® products, including other varieties of Edible cookie dough or Ready-to-Bake cookie dough.

While no illnesses or injuries have been reported, we took action out of an abundance of caution after a small number of consumers contacted Nestlé USA about this issue.

NESTLÉ® TOLL HOUSE® Edible Chocolate Chip Cookie Dough Tub - Product Packaging

Batch Codes:
22135554RR
22145554RR
22155554RR

Corresponding Best By Dates:
1/28/2023
1/29/2023
1/30/2023

Consumers who may have purchased these three batch codes (22135554RR, 22145554RR, 22155554RR) of Edible Chocolate Chip Cookie Dough tubs from NESTLÉ® TOLL HOUSE® should not consume the product and should return the product to the retailer where it was purchased for a replacement or refund. For any further support needed, please contact Nestlé USA at (800) 681-1678 Monday-Friday from 9 a.m.-6 p.m. EST.

Nestlé recently initiated a separate and unrelated recall for NESTLÉ® TOLL HOUSE® Stuffed Chocolate Chip Cookie Dough with Fudge Filling. Following each instance, we took immediate action to address the specific issue. We work closely with our suppliers and factory teams to ensure that our products are safe and meet the expectations of our consumers.

We are working with the U.S. Food & Drug Administration (FDA) on this voluntary recall and will cooperate with them fully.

The quality, safety and integrity of our products remain our number one priority. We sincerely apologize for any inconvenience this action represents to both our consumers and retail customers.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nestle-usa-announces-voluntary-recall-limited-quantity-edible-chocolate-chip-cookie-dough-tubs

Clorox® Recalls Pine-Sol® Scented Multi-Surface Cleaners, CloroxPro® Pine-Sol® All Purpose Cleaners, and Clorox® Professional™ Pine-Sol® Lemon Fresh Cleaners Due to Risk of Exposure to Bacteria

November 1, 2022

More Information: This recall involves Pine-Sol Scented Multi-Surface Cleaners in Lavender Clean, Sparkling Wave, and Lemon Fresh scents, CloroxPro Pine-Sol All Purpose Cleaners, in Lavender Clean, Sparkling Wave, Lemon Fresh, and Orange Energy scents, and Clorox Professional Pine-Sol Lemon Fresh Cleaners, with date codes beginning with the prefix “A4” and the first five digits numbered less than 22249. The products are sold in bottles of 28, 48, 60, 100, 144, and 175 fluid ounces. In an abundance of caution, Clorox is recalling all of the above-described products manufactured at its Forest Park, Georgia facility through September 2022.

Remedy:
Consumers should immediately stop using Pine-Sol Scented Multi-Surface Cleaners in Lavender Clean, Sparkling Wave, and Lemon Fresh scents, CloroxPro Pine-Sol All Purpose Cleaners, in Lavender Clean, Sparkling Wave, Lemon Fresh, and Orange Energy scents, and Clorox Professional Pine-Sol Lemon Fresh Cleaners that have date codes printed on the bottle beginning with “A4” and the first five digits numbered less than 22249, which represents products produced prior to September 2022. Consumers should take pictures of the 12-digit UPC code and the date code, dispose of the product in its container with household trash, and contact Pine-Sol for a full refund of the purchase price, with receipt, or of the manufacturer’s suggested retail price, without receipt.

Incidents/Injuries:
None reported

Sold At:
Online at Amazon.com and additional retailer websites and at Walmart, Sam’s Club, Dollar General, Target, Home Depot, BJ’s, Kroger, Dollar Tree, Lowe’s, Publix, and other major retailers nationwide, for between $2.50 and $12.50.

Manufacturer(s):
The Clorox Company, of Oakland, California.

Manufactured In:
United States

https://www.cpsc.gov/Recalls/2023/Clorox-Recalls-Pine-Sol-Scented-Multi-Surface-Cleaners-CloroxPro-Pine-Sol-All-Purpose-Cleaners-and-Clorox-ProfessionalTM-Pine-Sol-Lemon-Fresh-Cleaners-Due-to-Risk-of-Exposure-to-Bacteria-1

Nestlé USA Announces Voluntary Recall of NESTLÉ® TOLL HOUSE® STUFFED Chocolate Chip Cookie Dough with Fudge Filling Products Due to Potential Presence of Foreign Material

October 17, 2022

More Information: Nestlé USA is initiating a voluntary recall of ready-to-bake refrigerated NESTLÉ® TOLL HOUSE® STUFFED Chocolate Chip Cookie Dough with Fudge Filling products due to the potential presence of white plastic pieces.

This voluntary recall is isolated to NESTLÉ® TOLL HOUSE® STUFFED Chocolate Chip Cookie Dough with Fudge Filling products that were produced between June and September 2022. These products were distributed in the continental United States and Puerto Rico.

No other Nestlé Toll House products, including other NESTLÉ® TOLL HOUSE® STUFFED Cookie Dough and NESTLÉ® TOLL HOUSE® refrigerated cookie dough products, are impacted by this recall.

While no illnesses or injuries have been reported, we immediately took action out of an abundance of caution after a small number of consumers contacted Nestlé USA about this issue.

Consumers who may have purchased NESTLÉ® TOLL HOUSE® STUFFED Chocolate Chip Cookie Dough with Fudge Filling should not prepare or consume the product and should return the product to the retailer where it was purchased for a replacement or refund. For any further support needed, please contact Nestlé USA at (800) 681-1676 Monday-Friday from 9 a.m.-6 p.m. EST.

We are working with the U.S. Food & Drug Administration (FDA) on this voluntary recall and will cooperate with them fully.

The quality, safety and integrity of our products remain our number one priority. We sincerely apologize for any inconvenience this action represents to both our consumers and retail customers.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nestle-usa-announces-voluntary-recall-nestler-toll-houser-stuffed-chocolate-chip-cookie-dough-fudge

Hammond’s Candies Issues Allergy Alert on Undeclared Peanut in Salted Caramel Cookies

October 17, 2022

More Information: Hammond’s Candies of Denver, CO is recalling 5-ounce boxes of Hammond’s Salted Caramel Cookies, because they may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.

The product was distributed nationwide in retail stores and through mail orders.

The recalled Hammond’s Salted Caramel Cookies are packaged in a 5-ounce printed cardstock box, with UPC -6 91355 89889 5. Hammond’s item number for this product is CK15008. The recalled product code, “Best By: 6/29/2023A" can be found on a sticker and it is located at the lower-right corner of the back of the box.

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

The recall was initiated after a routine product check revealed that peanut-containing product had been packed and distributed in incorrect packaging, which did not declare the presence of peanuts. Further investigation has determined the root cause to be a temporary failure of the manufacturer’s packing and product release process.

Consumers who have purchased 5-ounce packages of Salted Caramel Cookies from the described lot are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Devon DeVries at Hammond’s Candies at 1-888-226-3999, Monday-Friday, 8am-4pm MST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hammonds-candies-issues-allergy-alert-undeclared-peanut-salted-caramel-cookies

Abbott Voluntarily Recalls Certain Lots of 2 Fl. Oz./59 mL Bottles of Ready-to-Feed Liquid Products

October 14, 2022

More Information: Abbott is initiating a proactive, voluntary recall of certain lots of 2 fluid ounce/59 milliliter bottles of Ready-to-Feed liquid products for infants and children, including the brands Similac® Pro-Total ComfortTM, Similac® 360 Total Care®, Similac 360 Total Care Sensitive, Similac® Special Care® 24, Similac Stage 1, Similac® NeoSure®, Similac Water (Sterilized) and Pedialyte Electrolyte Solution. The products included in the recall were manufactured at our Columbus, Ohio, manufacturing facility.

These products are being recalled because a small percentage of bottles (less than 1%) in the recalled lots have bottle caps that may not have sealed completely, which could result in spoilage. If spoiled product is consumed, gastrointestinal symptoms such as diarrhea and vomiting may occur.

This recall does not include any other liquid or powder formula brands or other nutrition products produced in our Columbus facility or elsewhere within our global nutrition manufacturing network. It also does not include any amino acid-based formulas or metabolic nutrition formulas.

This recall equates to less than one day's worth of the total number of ounces of infant formula fed in the U.S. and is not expected to impact the overall U.S. infant formula supply. Abbott is continuing production of Similac 2 fluid ounce/59 milliliter Ready-to-Feed liquid formula products for hospitals and healthcare providers' offices on a different production line. Similac infant formula will continue to be produced in alternative product sizes and formats for delivery to retail locations, in addition to increased production throughout our global manufacturing network.

The products included in the recall were distributed primarily to hospitals and to some doctors’ offices, distributors and retailers in the U.S., including Puerto Rico; one lot of products was sent to Barbados, Bermuda, Colombia, the Dominican Republic, Haiti, Jamaica, St. Croix and St. Thomas; and two lots were sent to Canada, Curacao, Panama, and Trinidad and Tobago

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/abbott-voluntarily-recalls-certain-lots-2-fl-oz59-ml-bottles-ready-feed-liquid-products-recall-not

AdvancePierre Foods Inc. Recalls Pork Fritter Product Due to Possible Foreign Matter Contamination

October 17, 2022

More Information

AdvancePierre Foods Inc., an Enid, Okla. establishment, is recalling approximately 4,137 pounds of pork loin steak fritter product that may be contaminated with extraneous materials, specifically hard pieces of plastic, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The raw, frozen cubed pork loin steak fritter item was produced on June 16, 2022. The following product is subject to recall [view label]:

10.14-lbs. bulk cases containing 27 pieces of “GOLD LABEL AdvancePierre Our Deluxe Cubed Pork Loin Streak Fritters” and lot code 1672AFE06.

The product subject to recall bears establishment number “EST. 2260Y” inside the USDA mark of inspection. This item was shipped to distributors in Arkansas, Colorado, Illinois, Indiana, Iowa, Michigan, Missouri, Nebraska and Virginia and further distributed to restaurants and other food service operations.

The problem was discovered after the firm notified FSIS that it had received two complaints from restaurant staff reporting they found hard pieces of plastic 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 the refrigerators and/or freezers of restaurants and food service operators. Restaurants and food service operators are urged not to serve this product. This product should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution 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 Kelly Hellbusch, Media Relations Manager, AdvancePierre, at 281-799-9784. Consumers with questions about the recall can call or text AdvancePierre at 855-382-3101, M-F from 8 a.m. to 5 p.m. CDT.

https://www.fsis.usda.gov/recalls-alerts/advancepierre-foods-inc--recalls-pork-fritter-product-due-possible-foreign-matter

Craftology, LLC DBA Dutch Treat Foods Issues Allergy Alert on Undeclared Cashews in “Craftology This is My Happy Place Pasta Salad”

October 12, 2022

More Information

Craftology, LLC dba Dutch Treat Foods of Zeeland, MI, is recalling its 14 ounce containers of “Craftology This Is My Happy Place Pasta Salad” because they may contain undeclared cashews. People who have allergies to cashews run the risk of serious or life-threatening allergic reaction if they consume these products.

The recalled “Craftology This Is My Happy Place Pasta Salad” was distributed in the midwestern United States in retail stores.

The product comes in a 14 ounce clear plastic clamshell package with a single label wrapped around on the top, side, and bottom of the container. Each container is marked on a clear side of the package with the following use by and lot code combinations:

USE BY: 10-04-22

LOT: 223008

USE BY: 10-12-22

LOT: 220709

USE BY: 10-14-22

LOT: 220909

USE BY: 10-18-22

LOT: 221309

USE BY: 10-20-22

LOT: 221509

USE BY: 10-25-22

LOT: 222009

USE BY: 10-27-22

LOT: 222209

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

This recall is not arising out of a food safety hazard caused by Craftology, LLC dba Dutch Treat Foods (“Company”). Company sources sunflower seeds from Lipari Foods Operating Company (“Lipari”), which sources that ingredient from Shah Trading Company Limited (“Shah Trading”). On October 5, 2022, Lipari, a distributor of Shah Trading products, initiated a recall of sunflower seeds that Company uses in the above referenced product due to an undeclared allergen, Cashew, which was discovered in a case of the Sunflower Seeds Oil RS bulk product produced by Shah Trading. Accordingly, Company is issuing a voluntary recall of product that contain the affected lot of the Shah Trading sunflower seeds. There have been no confirmed reports of adverse reactions due to consumption of Company’s product.

Consumers who have purchased 14 ounce packages of "Craftology This Is My Happy Place Pasta Salad" are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 616-772-5921 Monday through Friday, 7AM to 3PM EST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/craftology-llc-dba-dutch-treat-foods-issues-allergy-alert-undeclared-cashews-craftology-my-happy?utm_medium=email&utm_source=govdelivery

Lipari Foods Issues Voluntary Product Recall of Specific Sesame Sticks Mix and Roasted/Salted Sunflower Meat Tubs Due to Undeclared Cashew Allergen

October 11, 2022

More Information

Lipari Foods has issued a voluntary recall of specific lots of sesame sticks mix and roasted and salted sunflower meat tub products packaged by sister company JLM due to an undeclared cashew (tree nut) 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 products were distributed to retail stores throughout Florida, Georgia, Illinois, Indiana, Kentucky, Maryland, Michigan, Minnesota, Missouri, North Carolina, New York, Ohio, Oklahoma, Pennsylvania, Texas, Tennessee, Wisconsin, and West Virginia.

Products were distributed as generic product without branding.

The affected products can be identified by:

Brand

Product

Lipari Product #

Size

Lot Code

Best By Date

UPC

JLM TUB

SESAME STICKS MIX

368268

11 oz.

08202209B
13202209B

03/07/23
03/12/23

094776081646

JLM TUB

SUNFLOWER MEAT
ROASTED/SALTED

210903

10 oz.

09202209B
12202209B

03/08/23
03/11/23

760208118135

There are no reported illnesses in connection with these products to date.

This was brought to our attention by our sister company, JLM after they discovered cashews (tree nuts) in the bulk Oil Roasted and Salted Sunflower Seeds product from their bulk supplier, Shah Trading Co. The bulk product was used to package the Sesame Sticks Mix and Roasted/Salted Sunflower Meat Tub products. Lipari Foods non-branded products are being recalled as they may contain an undeclared allergen. We are working closely with the FDA to ensure that all potentially impacted product has been pulled from commerce.

Consumers who have purchased this recalled product should not consume it. They should return it to the point of purchase. Consumers with questions should call Customer Service at 800-729-3354, 8:15 am – 4:30 pm, EST, Monday through Friday.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lipari-foods-issues-voluntary-product-recall-specific-sesame-sticks-mix-and-roastedsalted-sunflower

Bakkavor USA Issues Allergy Alert for 32 Ounce Meal Simple Tomato Basil Soup for Mislabeling and Undeclared Dairy

October 7, 2022

More Information: Bakkavor USA of Jessup, Pennsylvania, is initiating a proactive, voluntary recall of the 32-ounce Meal Simple Tomato Basil Soup as it has been mislabeled and may contain undeclared dairy. People who have an allergy or severe sensitivity to dairy run the risk of a serious or life-threatening allergic reactions if they consume the product. The 32-ounce Meal Simple Tomato Basil Soup with the 12/2/2022 best date was sold at H-E-B stores in Texas with a label stating Meal Simple Beef Chili With Beans.

The recall was initiated after it was discovered that the front label was mislabeled for the 32-ounce Meal Simple Tomato Basil Soup, produced on 9/15/2022 with best by date of 12/2/2022 and does not contain an allergen declaration of milk, which is found in the product. The root cause investigation is ongoing and there have been no known reports of adverse reactions.

Consumers who have purchased 32-ounce Meal Simple Beef Chili with Beans or Meal Simple Tomato Basil Soup are urged to return it to the place of purchase for a full refund. Consumers with questions may contact H-E-B Customer Service at 1-855-432-4438 Monday through Friday from 8 a.m. to 5 p.m. Central Standard Time.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bakkavor-usa-issues-allergy-alert-32-ounce-meal-simple-tomato-basil-soup-mislabeling-and-undeclared

Cut Fruit Express Recalls Caribou Coffee Fruit and Cheese Plate Because of Possible Health Risk

October 7, 2022

More Information: Cut Fruit Express of Inver Grove Heights, MN is recalling Caribou Coffee Fruit and Cheese Plate 6.2oz because of potential contamination 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.

Caribou Coffee Fruit and Cheese Plate, item #3818, was distributed from Caribou Stores at the MSP Airport Caribou locations in the MSP Airport, Minnesota. The product comes in a clear plastic package. The USED BY DATES are 9/30/2022, 10/2/2022, 10/4/2022, 10/7/2022 and 10/9/2022.

Cut Fruit Express learned that their supplier is issuing a recall on Brie Cheese for potential contamination of Listeria Monocytogenes. Cut Fruit Express is initiating a recall on the affected product that contains the recalled Brie Cheese. The affected products were shipped between September 26th through October 5th, 2022.

Consumers should immediately DESTROY THE PRODUCT if they have it in their possession. Please do not share or give it to anyone to eat. Consumers who have purchased 6.2oz snack packages of Fruit and cheese plate may return them to the place of purchase for a full refund.

Consumers with questions may contact
Shelley M. Ryan
Partner | 952.746.2705 Hoff Barry, P.A.
100 Prairie Center Drive, Suite 200
Eden Prairie, MN 55344 952.941.9220 | hoffbarry.com weekdays from 9:00 - 5:00 Central Time.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/cut-fruit-express-recalls-caribou-coffee-fruit-and-cheese-plate-because-possible-health-risk

Flowers Foods Issues Allergy Alert on Undeclared Soy in Certain TastyKake and Mrs. Freshley’s Glazed Pies

October 7, 2022

More Information

Flowers Foods, Inc. (NYSE: FLO) is voluntarily recalling Tastykake® and Mrs. Freshley’s® glazed pies due to 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 product.

The products being recalled were distributed from Sept. 26, 2022 through Oct. 6, 2022 to retail and vending customers throughout the U.S., Canada, and Mexico. The packages have either an “Enjoy By” date of 10/28/2022 through 11/07/2022 and/or product codes 307 2263 through 307 2274 printed on the front of the packages. The UPC codes are printed on the back of the packages.

The recall was initiated after discovering that certain pies were made with an ingredient containing soy, which is not listed on the product label. No related illnesses or incidents have been reported to date.

Following is information about the products involved in the recall. People allergic to soy should not consume products if the “Enjoy By” dates, UPC and/or Product Codes below are printed on the package.

Product Description

UPC #

"Enjoy By" Dates

or Product Codes

Mrs. Freshley's Apple Fruit Pie

0-72250-00817-4
0-72250-07393-6

Oct. 28, Oct. 31,
Nov. 4, and Nov. 7

307 2263 through 307 2274

Mrs. Freshley's Cherry Fruit Pie

0-72250-00815-0

Oct. 28, Oct. 31,
Nov. 4, and Nov. 7

307 2263 through 307 2274

Tastykake Glazed Apple Pie

0-25600-00972-7

Oct. 28, Oct. 31,
Nov. 4, and Nov. 7

307 2263 through 307 2274

Tastykake Glazed Caramel Apple Pie

0-25600-08618-6

Oct. 28, Oct. 31,
Nov. 4, and Nov. 7

307 2263 through 307 2274

Tastykake Glazed Cherry Pie

0-25600-00969-7

Oct. 28, Oct. 31,
Nov. 4, and Nov. 7

307 2263 through 307 2274

Tastykake Glazed Lemon Flavored Pie

0-25600-00967-3

Oct. 28, Oct. 31,
Nov. 4, and Nov. 7

307 2263 through 307 2274

Tastykake Variety Glazed Pie Shipper – contains:
- Tastykake Glazed Apple Pie
- Tastykake Glazed Cherry Pie
- Tastykake Glazed Lemon Flavored Pie

0-72250-00817-4
0-25600-00969-7
0-25600-00967-3

Oct. 28, Oct. 31,
Nov. 4, and Nov. 7

307 2263 through 307 2274

Affected product should be discarded or may be returned to the place of purchase for a full refund. Consumers with questions may call Flowers’ Consumer Relations Center at 1-866-245-8921. The center is open Monday through Friday from 8:00 a.m. to 5:00 p.m. Eastern Standard Time. Consumers also may contact the center via e-mail by visiting www.flowersfoods.com/contact/consumers.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/flowers-foods-issues-allergy-alert-undeclared-soy-certain-tastykake-and-mrs-freshleys-glazed-pies

Cuisine Innovations Unlimited, LLC Issues Voluntary Recall of Two Varieties of Earth Grown Frozen Falafel Due to Possible Health Risk

October 7, 2022

More Information: Cuisine Innovations Unlimited, LLC of 180 Lehigh Avenue, Lakewood, NJ, is voluntarily recalling its Earth Grown Vegan Traditional Falafel and Garlic & Herb Falafel Distributed & Sold Exclusively by Aldi, Batavia, IL due to the possible presence of Shiga toxin-producing E. coli.

Shiga-toxin-producing E. coli is an organism that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include stomach cramps, diarrhea, and vomiting. The illness primarily impacts elderly individuals, children, and people with weakened immune systems. Most healthy adults and children rarely become seriously ill.

The voluntarily recalled Earth Grown Vegan Traditional Falafel And Garlic & Herb Falafel Distributed & Sold Exclusively by Aldi, Batavia, IL were distributed in ALDI retail stores in the following states: Alabama, Arizona, Arkansas, California, Connecticut, Delaware, District of Columbia, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New Hampshire, New Jersey, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, West Virginia, and Wisconsin.

The product comes in a bag in a box marked with any of the following Lot numbers: 1472, 1481, 1531, 1532, 1541, 1552, 1561, 1581, 1601, 1611, 1612, 1661, 1682, 1732, 1752, 1762, 1782, 1802, and 1812, and would have been shipped to stores after June 24, 2021. The lot number can be found in the “Best if used by” area on the outside flap of the box. There has been no further production of this product.

There have been 20 reported cases in six (6) states (FL, IA, KS, MI, OH and WI) with onset dates reported between July 24 and September 19, 2022 with 5 hospitalization and no deaths.

Consumers who have purchased Earth Grown Vegan Traditional Falafel and Garlic & Herb Falafel Distributed & Sold Exclusively by Aldi, Batavia, IL with any of the above lot numbers after June 24, 2021, are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company Monday through Friday, 8:00 a.m. to 4:00 p.m. Eastern Time at 1-201-439-1036, Ext. 26.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/cuisine-innovations-unlimited-llc-issues-voluntary-recall-two-varieties-earth-grown-frozen-falafel

Old Europe Cheese, Inc. EXPAND Voluntary Recall of Its Brie Cheeses Due to Possible Health Risk

October 5, 2022

More Information

Old Europe Cheese, Inc. of Benton Harbor, MI is expanding its voluntary recall of Brie cheeses announced on September 30, 2022, because of potential contamination with Listeria monocytogenes, to include additional products, specifically baked brie cheeses. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

RECALL DETAILS
The following baked brie products are being added to the 9/30/2022 Old Europe Cheese voluntary recall. These are products with best by dates through 12/14/2022 and are subject to the voluntary recall. The products were distributed from August 01, 2022 through September 28, 2022 and were available at supermarkets, wholesale and retail stores nationwide and Mexico.

The following products being recalled are marked with Best By Dates ranging from September 28, 2022 to December 14, 2022.

Brand

Product Name

Packaging & Size

UPC Code

CULINARY TOUR

*8 oz Plain Baked Brie

Clamshell 8 oz

011225005350

CULINARY TOUR

*11 oz Cranberry Baked Brie

Clamshell 11 oz

011225005367

LA BONNE VIE

*8 oz Plain Baked Brie

Clamshell 8 oz

820581678814

LA BONNE VIE

*11 oz Cranberry Baked Brie

Clamshell 11 oz

820581678821

LIDL

* 8 oz Plain Baked Brie

Clamshell 8 oz

4056489151203

LIDL

*11 oz Cranberry Baked Brie

Clamshell 11 oz

4056489151203

LIDL

*11 oz Fig Baked Brie

Clamshell 11 oz

4056489310907

PRIMO TAGLIO

* 8 oz Plain Baked Brie

Clamshell 8 oz

021130098460

Reny Picot

*8 oz Plain Baked Brie

Clamshell 8 oz

033421050088

Reny Picot

*11 oz Cranberry Baked Brie

Clamshell 11 oz

033421051115

Reny Picot

*11 oz Apple Baked Brie

Clamshell 11 oz

033421500811

Reny Picot

*11 oz Fig Baked Brie

Clamshell 11 oz

033421053119

Consumers who have purchased the stated products are urged not to consume it and discard the product. FDA recommends in these cases that anyone who purchased or received any recalled products to use extra vigilance in cleaning and sanitizing any surfaces and containers that may have come in contact with these products to reduce the risk of cross-contamination. Listeria can survive in refrigerated temperatures and can easily spread to other foods and surfaces.

Old Europe Cheese has set up a telephone line to answer any questions about this recall, The number is 269-925-5003 ext 335 and is open Monday through Friday from 9:00am-12:30pm and 2:00pm-4:00pm ET.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/old-europe-cheese-inc-expands-voluntary-recall-its-brie-cheeses-due-possible-health-risk

Diana’s Bananas Issues Allergy Alert on Undeclared Peanuts in Milk Chocolate Banana Babies

September 30, 2022

More Information: Diana’s Bananas, LLC of Chicago is announcing an allergy alert and voluntary recall of its 10.5-ounce packages of Milk Chocolate Banana Babies dipped frozen bananas that may contain undeclared peanuts. People who have allergies to peanuts run the risk of a serious or life- threatening allergic reaction if they consume these products.

The voluntary recall comes after it was discovered that the product was distributed in packaging that did not reveal the presence of peanut butter.

The recalled Banana Babies Milk Chocolate were distributed to six specific retailers/distributors (Stater Brothers, San Bernardino, California; Albertsons/Safeway Irvine, California; Kroger Syracuse, Utah; Lipari Foods, Warren, Michigan; UNFI Iowa City, Iowa; UNFI, Ridgefield, Washington).

The product comes in a 10.5-ounce, blue box marked with a BEST IF USED BY DATE of C 08 05 23 on the top of the pull tab. The UPC code is- 7-43490-00010-4.

Consumers who have purchased 10.5-ounce packages of Milk Chocolate Banana Babies with a “BEST IF USED BY” date of C 08 05 23 are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Diana’s Bananas from 9 a.m. to 5 p.m. Central Standard Time, Monday through Friday, at 1-800-848-3641 or by emailing customer-service@dianasbananas.com.

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

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dianas-bananas-issues-allergy-alert-undelcared-peanuts-milk-chocolate-banana-babies

Swiss American Participates in Manufacturer Old Europe’s Recall of Brie and Camembert

October 4, 2022

More Information: Old Europe Cheese, Inc. of Benton Harbor, MI is issuing a voluntary recall of its Brie cheeses because of potential contamination 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.

Swiss American is recalling St Louis Brie products after being alerted by the manufacturer Old Europe Cheese, Inc. that the products could be contaminated with Listeria monocytogenes. This is part of a voluntary broader recall by the manufacturer.

Customers are urged to check for:
St Louis Domestic Brie Wedge
7 oz
UPC: 041563 263709
All dates up to and including 12/14/2022

St Louis Domestic Cut Brie Wedge-6 lb RW
Variable weight
UPC: 041563 370018
All dates up to and including 12/14/2022

St Louis Brie
Variable Weight
UPC: 21107100000
All dates up to and including 12/14/2022

ST LOUIS BRIE PRE CUT WEDGES
Code Date: best by dates through 12/14/2022
Size: 16.00 OZ
UPC: 00021565000000

ST LOUIS CW BRIE WHEEL
Code Date: best by dates through 12/14/2022
Size: 16.00 OZ
UPC: 00021171800000

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/swiss-american-participates-manufacturer-old-europes-recall-brie-and-camembert?utm_medium=email&utm_source=govdelivery

Whole Foods Market Issues Allergy Alert for Zerto Fontal Cheese Sold in Connecticut, New Jersey, and New York

September 30, 2022

More Information: Whole Foods Market is voluntarily recalling Zerto Fontal cheese from fifty-four stores in Connecticut, New Jersey and New York because the product contains egg lysozyme, an egg white protein, which is not declared on the product label. People who have an allergy or severe sensitivity to eggs run the risk of a serious or life-threatening allergic reaction if they consume these products.

The affected product was sold at Whole Foods Market locations in New York, Connecticut, and New Jersey. The products were located in the Specialty department and were packaged by the slice with Whole Foods Market scale labels. The affected products can be identified by the name “Zerto Fontal”, a product code of 20565300000, sell by dates of 9/21/2022 – 10/20/2022, and were available for purchase from 9/21/2022 through 9/29/2022.

All affected product has been removed from store shelves. The mislabeling issue was discovered by a customer complaint of illness.

Customers who purchased this product at Whole Foods Market can bring a valid receipt into stores for a full refund. Customers with additional questions can call 1-844-936-8255 daily between the hours of 6:00 a.m. and 12:00 a.m. CST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-zerto-fontal-cheese-sold-connecticut-new-jersey-and-new-york?utm_medium=email&utm_source=govdelivery

The Chai Box Announces Voluntary Recall of Chai Concentrate Mix and Chai Concentrate Unsweetened Mix Due to Potential Clostridium Botulinum Contamination

September 29, 2022

More Information: Marietta, GA, September 29, 2022 – The Chai Box announced a recall of 16 oz glass bottles Chai Concentrate Mix, UPC 7 93611 81925 2 and 64 oz plastic bottles of Chai Concentrate Mix UPC 7 93611 81926 9 and 16 oz glass bottles Unsweetened Chai Concentrate Mix, UPC 793611819252 and 64 oz plastic bottles of Unsweetened Chai Concentrate Mix UPC 793611819269 due to potential under-processing which may lead to Clostridium botulinum contamination. These deviations were part of the commercial sterilization process and could result in contamination by spoilage organisms or pathogens, which could lead to life-threatening illness if consumed. No other production codes or products are affected by this recall.

It is important to note that there have been no reports of illness associated with this product to date.

The products subject to recall are 16 oz glass bottles and 64 oz plastic bottles with Best By dates between 09/22/2022 and 03/16/2023. Please see that attached photos for ease of identification of the products.

We were notified of the problem during a process review by the Georgia Department of Agriculture. The products were shipped nationwide to consumers, retailers and wholesalers. Some product was also shipped to two consumers in Canada. Product is available online and via retail and wholesale facilities.

The Best By date is either etched on the bottles or on a sticker is located on the bottom or side of the bottles. If consumers have any product with the indicated “Best By” dates, they should return it to the place of purchase for a full refund or exchange. Consumers with questions may contact the company by calling 844-242-4269, Monday-Friday, 9:00 am – 5:00 pm Eastern Time or by emailing at recall@thechaibox.com.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/chai-box-announces-voluntary-recall-chai-concentrate-mix-and-chai-concentrate-unsweetened-mix-due

Old Europe Cheese, Inc. Issues Voluntary Recall of Its Brie and Camembert Cheeses Due to Possible Health Risk

September 30, 2022

More Information

Old Europe Cheese, Inc. of Benton Harbor, MI is issuing a voluntary recall of its Brie and Camembert cheeses because of potential contamination 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.

RECALL DETAILS
All Old Europe Cheese Brie and Camembert products with best by dates through 12/14/2022 are subject to the voluntary recall. The products were distributed from August 01, 2022 through September 28, 2022 and were available at supermarkets, wholesale and retail stores nationwide and Mexico; retailers include Albertsons, Safeway, Meijer, Harding’s, Shaw’s, Price Chopper, Market Basket, Raley’s, Save Mart, Giant Foods, Stop & Shop, Fresh Thyme, Lidl, Sprouts, Athenian Foods, Whole Foods. This list may not include all retail establishments that have received the recalled product or may include retail establishments that did not actually receive the recalled product.

The following products being recalled are marked with Best By Dates ranging from September 28, 2022 to December 14, 2022, Retailers may have repackaged bulk Old Europe Cheese items into smaller containers and sold this repackaged product to consumers. This repackaged product may not bear the original labeling and product information as described below:

Brand

Product Name

UPC Code

BLACK BEAR

6 lb Black Bear Wheel

N/A

BLOCK AND BARREL

2.2 lb Block and Barrel Brie

078982603281

BLOCK AND BARREL

6.6 lb Block and Barrel Brie

N/A

CHARMANT

2.2 lb Brie - double crème, whole wheel - CHARMANT

N/A

CHARMANT

8 oz Brie - double crème, rounds

033421023860

COBBLESTONE

2.2 lb Cobblestone Brie Wheel

822486179809

CULINARY TOUR

8 oz Brie - double crème, rounds

011225005145

CULINARY TOUR

8 oz Brie - double crème, wedges, saran wrapped

N/A

FREDERICKS

8 oz Brie - dbl crème, wedges, saran wrapped

N/A

FREDERICKS

8 oz Brie - triple crème, rounds

708820301214

FRESH THYME

8 oz Brie - double crème, rounds

841330111994

FRESH THYME

8 oz Brie - triple crème, rounds

841330111987

FRESH THYME

8 oz Brie - wedges, saran wrapped

N/A

FRESH THYME

8 oz Camembert-Traditionnel rounds

841330111970

GLENVIEW FARMS

2.2 lb Brie - double crème, whole wheel

758108121355

GLENVIEW FARMS

3.25 lb Brie-double crème, rectangular RW

758108670150

GOOD AND GATHER

8 oz Good and Gather Wheel

085239047620

HEINEN

8 oz Brie - triple crème, rounds

020601418028

JOAN OF ARC

14 oz Joan of Arc Brie Wheel

711565129111

JOAN OF ARC

2.2 lb Joan of Arc Herb and Garlic Wheel

N/A

JOAN OF ARC

2.2 lb Joan of Arc Peppercorn Wheel

N/A

JOAN OF ARC

6.5 lb Joan of Arc Triple Creme Wheel

N/A

JOAN OF ARC

8 oz Joan of Arc Camembert Wheel

711565112243

JOAN OF ARC

8 oz Joan of Arc Double Cream Wedge

711565204993

JOAN OF ARC

8 oz Joan of Arc Double Creme Wheel

711565112236

JOAN OF ARC

8 oz Joan of Arc Slicing Brie

711565200520

JOAN OF ARC

8 oz Joan of Arc Triple Creme Wheel

711565129104

LA BONNE VIE

14 oz Brie - double crème, rounds

820581678678

LA BONNE VIE

2.2 lb Brie - double crème, whole wheel

820581678685

LA BONNE VIE

6.5 lb Brie - double crème, whole wheel RW

820581678692

LA BONNE VIE

7 oz Brie - dbl crème w/Herbs, wedges, foil wrapped

820581678661

LA BONNE VIE

7 oz Brie - double crème, wedges, foil wrapped

820581678654

LA BONNE VIE

8 oz Brie - double crème, rounds

820581678531

LA BONNE VIE

8 oz Brie - triple crème, rounds

820581678746

LA BONNE VIE

8 oz Camembert - double crème, rounds

820581678616

LIDL

8 oz Brie - double crème, rounds

4056489151739

LIFE IN PROVENCE

8 oz Brie - rounds

787984111952

MARKET 32

14 oz Brie - double crème, rounds

41735052865

MARKET 32

8 oz Brie - double crème, rounds

41735052834

MARKET 32

8 oz Brie - double crème, wedges, saran wrapped

41735052872

MARKET 32

8 oz Brie - triple crème, rounds

41735052858

MARKET 32

8 oz Brie-dbl crème w/Herbs, wedges, saran wrapped

41735052889

MARKET 32

8 oz Camembert - Traditionnel double crème, rounds

41735052841

MATRIE 'D

2.2 lb Matrie'd Wheel

780487488422

METROPOLITAN

6.5 lb Metropolitan Wheel

N/A

METROPOLITAN

8 oz Metropolitan Wheel

711565007679

PRESTIGE

8 oz Brie - triple crème, rounds

021140033635

PRIMO TAGLIO

6.5 lb Brie - w/Herbs, whole wheel

N/A

PRIMO TAGLIO

8 oz - w/Herbs, wedges

21004900002

PRIMO TAGLIO

8 oz Brie - double crème, rounds

021130045679

PRIMO TAGLIO

8 oz Brie - slicing rectangle

021130098453

PRIMO TAGLIO

8 oz Brie - triple crème, rounds - ST ROCCO

133421027865

RED APPLE

7 oz Brie - double crème, rounds

604262030005

RED APPLE

8 oz Brie - double crème, wedges, saran wrapped

604262030036

Reny Picot

1 lb Brie - double crème, slicing rectangle

033421024201

Reny Picot

14 oz Brie - double crème w/Herbs, rounds

033421022764

Reny Picot

14 oz Brie - double crème, rounds

033421022757

Reny Picot

14 oz Camembert - double crème, rounds

033421022795

Reny Picot

2.2 lb Brie - double crème, whole wheel

N/A

Reny Picot

2.2 lb Brie - triple crème, whole wheel

N/A

Reny Picot

3.25 lb Brie - double crème, rectangular

N/A

Reny Picot

6.5 lb Brie - double crème w/Herbs, whole wheel

N/A

Reny Picot

6.5 lb Brie - double crème, whole wheel RW - RENY PICOT

N/A

Reny Picot

6.5 lb Brie - triple crème, whole wheel

N/A

Reny Picot

6.5 lb Brie-dbl crème w/Peppercorn, whole wheel

N/A

Reny Picot

6.5 lb Camembert - double crème, whole wheel

N/A

Reny Picot

7 oz Brie - double crème w/Herbs, wedges, foil wrapped

033421022429

Reny Picot

7 oz Brie - double crème, rounds no cups

N/A

Reny Picot

7 oz Brie - double crème, wedges, foil wrapped

033421022417

Reny Picot

8 oz Brie - dbl crème w/Peppercorn, wedges, saran wrapped

N/A

Reny Picot

8 oz Brie - dbl crème, wedges, saran wrap RW

N/A

Reny Picot

8 oz Brie - double crème w/Herbs, wedges, saran wrapped

N/A

Reny Picot

8 oz Brie - double crème, rounds

033421022863

Reny Picot

8 oz Brie - double crème, slicing rectangle

033421024300

Reny Picot

8 oz Brie - double crème, wedges, saran wrapped

N/A

Reny Picot

8 oz Brie - triple crème, rounds - ST ROCCO

133421027865

Reny Picot

8 oz Brie - trpl crème, wedges, saran wrap RW - ST ROCCO

N/A

Reny Picot

8 oz Brie - wedges, saran wrapped

033421022313

Reny Picot

8 oz Camembert - double crème, rounds

033421022900

Reny Picot

8 oz Camembert - Traditionnel double crème, rounds

033421024904

ST RANDEAUX

14 oz Brie - double crème, rounds

636625003401

ST RANDEAUX

2.2 lb Brie - double crème, whole wheel

N/A

ST RANDEAUX

6.5 lb Brie - double crème, whole wheel RW

N/A

ST RANDEAUX

8 oz Brie - dbl crème w/Herbs, wedges, saran wrpd RW

N/A

ST RANDEAUX

8 oz Brie - dbl crème w/Pepper, wedges, saran wrpd RW

N/A

ST RANDEAUX

8 oz Brie - double crème, rounds

636625003418

ST RANDEAUX

8 oz Brie - triple crème, rounds

636625003548

ST RANDEAUX

8 oz Camembert - Traditionnel, rounds

636625003425

TASTE OF INSPIRATION

8 oz Brie - rounds

725439802550

TASTE OF INSPIRATION

8 oz Brie - triple crème, rounds

725439999731

TASTE OF INSPIRATION

8 oz Brie - w/Herb center layer, rounds

725439802567

TASTE OF INSPIRATION

8 oz Brie - wedges, saran wrapped

N/A

TRADER JOE

8 oz Trader Joe Slicing

00505086

Consumers who have purchased the stated Brie and Camembert products are urged not to consume it and discard the product. FDA recommends in these cases that anyone who purchased or received any recalled products to use extra vigilance in cleaning and sanitizing any surfaces and containers that may have come in contact with these products to reduce the risk of cross-contamination. Listeria can survive in refrigerated temperatures and can easily spread to other foods and surfaces.

Old Europe Cheese has set up a telephone line to answer any questions about this recall, The number is 269-925-5003 ext 335 and is open Monday through Friday from 9:00am-12:30pm and 2:00pm-4:00pm ET.

BACKGROUND
This action was triggered after a full environmental audit of 120 samples, both of the product and of the company’s facilities. None of the products showed contamination, but one of the facilities’ samples tested positive. The strain from that positive case has been linked to 6 cases of Listeriosis dating from 2017 to 2022. These cases were not previously linked to this company’s products, but Old Europe Cheese decided to do this voluntary recall in order to avoid any risk to their customers.

The Company has decided to voluntarily initiate the product recall based on these results and with a focus on their consumers’ health. The source of potential contamination has been identified and Old Europe Cheese is taking active measures to eliminate it. Production of these products has been stopped and will not restart until the Company has full confidence in the effectivity of the applied measures.

The company is working closely with state and federal authorities and with its clients to make this voluntary recall as fast and efficient as possible. The quality and safety of our products is our number one priority. We sincerely apologize for any inconvenience caused by this situation. Old Europe Cheese’s top priority is the health of our customers.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/old-europe-cheese-inc-issues-voluntary-recall-its-brie-and-camembert-cheeses-due-possible-health

FSIS Issues Public Health Alert for Ready-To-Eat Chili Cheese Wieners Due to Possible Listeria Contamination

October 1, 2022

More Information

The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert because Family Fare, a Chippewa Falls, Wisc. establishment, produced ready-to-eat chili cheese wieners that may be contaminated with Listeria monocytogenes. A recall was not requested because it is believed that the products are no longer in commerce.

The ready-to-eat chili cheese wieners were produced on Sept. 21, 2022. The following products are subject to the public health alert [view labels]:

15-oz. vacuum-packed packages containing “Our Local SMOKEHOUSE Chili Cheese flavored Wieners” with a use by date of January 19, 2023.

The products bear establishment number “695SEWI” inside the USDA mark of inspection. These items were shipped to a Family Fare retail location in Cannon Falls, Minnesota, where three packages of the wieners were sold.

The problem was discovered when the Wisconsin Department of Agriculture reported to FSIS that some product was found to be contaminated with Listeria monocytogenes during routine testing.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.

Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.

Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections can occur in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.

FSIS is concerned that some product may be in consumers’ refrigerators 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.

Media and consumers with questions regarding the public health alert can contact press@spartannash.com.

https://www.fsis.usda.gov/sites/default/files/food_label_pdf/2022-10/pha-label-10012022.pdf

Van Law Food Products Issues Allergy Alert on Undeclared Soy and Wheat in Product EXPANDED

September 23, 2022

More Information: VanLaw Food Products Inc. is expanding its recall of Whole Foods Market 365 Organic Creamy Caesar Dressing because it contains undeclared Soy and Wheat allergens. The recall is being expanded to include Whole Foods Market 365 Organic Creamy Caesar Dressing with a BEST IF USED BY DATE of SEP 21 22 through JUN 06 23 and incorrect UPC Code 99482-49027.

People who may have an allergy or severe sensitivity to Soy or Wheat run the risk of serious or life- threatening allergic reaction if they consume these ingredients. The recalled products were sold in the produce or dairy department and distributed nationwide through Whole Foods Markets. All affected product has been removed from store shelves.

No illnesses have been reported to date.

The recalls were initiated when it was discovered the products were distributed in packaging that did not reveal the presence of Soy and Wheat allergen. The problem was caused when the back label from another product was mistakenly put on the products being recalled.

Consumers who purchased Whole Foods Market 365 Organic Creamy Caesar Dressing bottles with these Used by Codes (UPC code 99482-49027) in 12oz glass bottles should discard the product and seek a refund at the point of sale. Consumers with additional questions can call 1-844-936-8255 between the hours of 7:00 am and 10:00 pm CST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/van-law-food-products-issues-allergy-alert-undeclared-soy-and-wheat-product-expanded?utm_medium=email&utm_source=govdelivery

TreeHouse Foods Announces Voluntary Recall of Certain Tuscan Garden Restaurant Style Italian Dressing Due to Undeclared Wheat and Soy

September 24, 2022

More Information

TreeHouse Foods, Inc. (NYSE: THS) is voluntarily recalling one lot of Restaurant Style Italian Dressing sold under the brand name Tuscan Garden.

This recall is being conducted because the product is labeled as Restaurant Style Italian Dressing, while some of the bottles may contain Asian Sesame Dressing. The Restaurant Style Italian Dressing label indicates the allergens egg and dairy are in the product while the Asian Sesame Dressing product contains the allergens soy and wheat. People who have an allergy or severe sensitivity to soy or wheat run the risk of serious or life-threatening allergic reaction if they consume this product.

Product was distributed nationwide through Aldi between August 23, 2022 and September 23, 2022.

The product at issue can be identified by the UPC number and best if used by date which can be found below the neck of the bottle.

Description

Size

UPC Number

Best If Used By Date

Tuscan Garden Restaurant Style Italian Dressing

16 oz

4099100074871

08/10/2023

Photos of the affected product label can be found below. No other varieties or UPC numbers are included in this recall.

TreeHouse Foods discovered the issue after receiving two complaints from the store level. At this time, TreeHouse has not received any reports of an allergic reaction associated with this product.

Consumers who have purchased any of the above products are urged to dispose of or return the products to the place of purchase for a full refund. Consumers with any questions may call 800- 596-2902, Monday through Friday between 8:00 a.m. and 7:00 p.m. (EST).

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/treehouse-foods-announces-voluntary-recall-certain-tuscan-garden-restaurant-style-italian-dressing?utm_medium=email&utm_source=govdelivery

Arcade Snacks Issues Allergy Alert on Undeclared Egg in Candy Corn

September 23, 2022

More Information

Arcade Snacks of Auburn, MA is recalling its 15 ounce packages of Candy Corn because they may contain undeclared egg. People who have allergies to egg run the risk of serious or life-threatening allergic reaction if they consume these products.

Candy Corn was distributed in Massachusetts and Connecticut at the following locations:

Johnson Roadside Farm Market in Swansea, Massachusetts
Donelan’s Supermarkets in Massachusetts
Fieldstone Farm Market in Marion, Massachusetts
Foodies in Massachusetts
Windfall Market in Falmouth, Massachusetts
Highland Park Market in Glastonbury, Connecticut

The product comes in a 15 ounce, clear plastic container marked with UPC #0 18586 00114 4 and a best by date of 3/8/2023 on the label on the back panel.

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

The recall was initiated after it was discovered that the egg-containing product was distributed in packaging that did not reveal the presence of egg.

Consumers who have purchased 15 ounce packages of Candy Corn are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-508-832-6300 Monday – Friday 8am – 5pm ET.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/arcade-snacks-issues-allergy-alert-undeclared-egg-candy-corn

Empanadas Valrico Inc. Recalls Beef and Chicken Empanada Products Produced Without Benefit of Inspection

September 23, 2022

More Information

Empanadas Valrico Inc., a Sarasota, Fla. establishment, is recalling approximately 6,247 pounds of beef and chicken empanada 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 beef and chicken empanada items were produced and distributed into commerce from March 2022 to September 2022. The following products are subject to recall [view labels]:

Approximately 1.6-lb. clear plastic bag packages containing 10 pieces of “Empanadas Valrico STEAK EMPANADAS” with “BEST BEFORE” dates prior to January 30, 2023.
Approximately 1.6-lb. clear plastic bag packages containing 10 pieces of “Empanadas Valrico CHICKEN EMPANADAS” with “BEST BEFORE” dates prior to January 30, 2023.
Approximately 4.6-lb. clear plastic bag packages containing 25 pieces of “Empanadas Valrico STEAK EMPANADAS” with “BEST BEFORE” dates prior to January 30, 2023.
Approximately 4.6-lb. clear plastic bag packages containing 25 pieces of “Empanadas Valrico CHICKEN EMPANADAS” with “BEST BEFORE” dates prior to January 30, 2023.

The products subject to recall do not bear the USDA mark of inspection because Empanadas Valrico Inc. is not a federally inspected establishment. These items were shipped to retail locations in Florida.

The problem was discovered when FSIS was notified by the Florida Department of Agriculture that the frozen empanada products did not have the USDA mark of inspection and were produced in an establishment that was not inspected by USDA.

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 Alfonso Bejarano, owner, Empanadas Valrico at (813) 408-0884 or empanadasvalrico@gmail.com.

https://www.fsis.usda.gov/recalls-alerts/empanadas-valrico-inc--recalls-beef-and-chicken-empanada-products-produced-without

Behrmann Meat and Processing Inc. Recalls Various Ready-to-Eat Meat Products Due to Possible Listeria Contamination

September 24, 2022

More Information: Behrmann Meat and Processing Inc., an Albers, Ill. establishment, is recalling approximately 87,382 pounds of various ready-to-eat (RTE) meat products that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. FSIS expects there to be additional product labels added in the near future and urges consumers to check back frequently to view updated labels.

The various RTE meat items were produced from July 7, 2022, to Sept. 9, 2022. The list of products and product codes for the RTE meat products that are subject to recall can be found here and includes all package sizes for all products with the affected lot codes. Available labels for the RTE meat products can be found here.

The products subject to recall bear establishment number “EST 20917” inside the USDA mark of inspection. These items were shipped to retail locations and wholesale distributors in Illinois, Kentucky, and Missouri.

The problem was discovered through product and environmental testing performed by FSIS and the establishment, which identified Listeria monocytogenes in the processing environment and in products produced by the establishment.

There have been no confirmed reports of illness or adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.

Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems can occur. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.

FSIS is concerned that some product may be in consumers’ pantries, refrigerators, or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Media and consumers with questions regarding the recall can contact Connie Haselhorst, VP Operations, Behrmann Meat and Processing Inc., at (618) 248-5151 or connie@behrmannmeats.com.

https://www.fsis.usda.gov/recalls-alerts/behrmann-meat-and-processing-inc--recalls-various-ready-eat-meat-products-due

World Variety Produce, Inc. Voluntarily Recalls Select Lots of Melissa’s Dutch Red Potatoes with Dijon Mustard Sauce Because it Contains Undeclared Egg Allergens

September 21, 2022

More Information

People with an allergy or severe sensitivity to Egg run the risk of serious or life-threatening allergic reaction if they consume this ingredient. The product was sold in the produce department and distributed in the states of Arizona, California, Florida, Iowa, Idaho, Kansas, Louisiana, Mississippi, Montana, New Jersey, Oklahoma, Texas, Utah, and Washington.

No illnesses have been reported to date.

Melissa’s Brand Dutch Red Potatoes with Dijon Mustard Sauce can be identified by the following descriptions:

Melissa’s Dutch Red Potatoes with Dijon Mustard Sauce

Brand

Melissa's

Packaging

Clear Overwrap Tray in Cardboard Sleeve

Pack/Weight

Net Weight 1LB 1.7OZ (502g)

UPC Code

0-45255-15221-0

Best Use By Dates

08/15/22, 08/20/22, 08/22/22, 08/29/22, 09/02/22, 09/05/22, 09/11/22, 09/18/22, 09/26/22,
10/01/22, 10/09/22

Consumers who have purchased Melissa’s Brand Dutch Red Potatoes with Dijon Mustard Sauce are urged to destroy and dispose of the recalled product. Consumers with questions may contact World Variety Produce, Inc. at 1-800-588-0151, Mon-Fri 7:00 AM–5:00 PM PST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/world-variety-produce-inc-voluntarily-recalls-select-lots-melissas-dutch-red-potatoes-dijon-mustard?utm_medium=email&utm_source=govdelivery

Salon Technologies, Inc. Issues Voluntary Nationwide Recall of Antica Ocean Citron Hand Sanitizer (Alcohol) Gel 65% Due to the Presence of Benzene

September 16, 2022

More Information

Salon Technologies International. Inc. is voluntarily recalling one lot of Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%, Lot 1166A. Expiration 6/18/2023 to the consumer level. Firm lab testing has found the product to contain benzene.

Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation , orally ,and through the skin. Depending on duration and level of exposure , it can result in cancers including leukemia, and blood cancer of the bone marrow and blood disorders which can be life-threatening. Salon Tech International, Inc. has not received any reports of adverse events related to this recall.

The product is used to help reduce bacteria , that potentially can cause disease , when soap and water are not available.

512 bottles of Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%, Lot 1166A, Expiration 6/18/2023 was distributed in the Seattle, Washington area.

Salon Technologies International. Inc. has notified its distributors by email and is arranging for return of all recalled products. Consumers that have product which is being recalled should stop using and return unused product to where it was obtained.

Consumers with questions regarding this recall can contact Salon Technologies International. Inc. by phone number ( 407-248-2948 ) or e-mail address salontechnologiesint@gmail.com , Monday to Friday 9am – 5pm , EST.

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: www.fda.gov/medwatch/report.htm
Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm 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.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/salon-technologies-inc-issues-voluntary-nationwide-recall-antica-ocean-citron-hand-sanitizer-alcohol?utm_medium=email&utm_source=govdelivery

Voluntary Recall of Certain Colgate Products Sold at Family Dollar Stores Because They Were Stored Outside of Temperature Requirements

September 16, 2022

More Information

Family Dollar is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and shipped to a limited number of stores in AZ, CA, GA, ID, IN, MT, NM, NV, OR, TX, and UT on or around May 1, 2022 through June 21, 2022 due to product being stored outside of labeled temperature requirements.

To date, Family Dollar is not aware of any consumer complaints or reports of illness related to this recall.

Products covered by this retail level recall include:

998277

COLGATE OPTIC WHITE STAIN PREVENTION TOOTHPASTE 2.1OZ

998909

COLGATE OPTIC WHITE CHARCOAL TOOTHPASTE 4.2OZ

999043

COLGATE OPTIC WHITE MOUTHWASH 16 FL OZ

999088

COLGATE OPTIC WHITE HIGH IMPACT TOOTHPASTE 3OZ

999749

COLGATE OPTIC WHITE TOOTHPASTE ICY FRESH 3.2OZ

999750

COLGATE OPTIC WHITE STAIN FIGHTER TOOTHPASTE CLEAN MNT 4.2OZ

Family Dollar has notified its affected stores asking them to check their stock immediately and to quarantine and discontinue the sale of any affected product. Customers that may have bought affected product may return such product to the Family Dollar store where they were purchased without receipt.

Customers with questions regarding this recall may contact Family Dollar Customer Service at 844-636-7687 between 9am and 5pm EST. Customers should contact their physician or health care provider if they have experienced any problems that may be related to using these products.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-certain-colgate-products-sold-family-dollar-stores-because-they-were-stored-outside?utm_medium=email&utm_source=govdelivery

GHGA Recalls Various Ready-To-Eat Vegetable Products Due to Possible Listeria Monocytogenes Contamination

September 20, 2022

More Information

GHGA is recalling various products (see chart below) due to the potential to be contaminated with Listeria monocytogenes. No other GHGA products are affected by this recall. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short- term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, a Listeria monocytogenes infection can cause miscarriages and stillbirths among pregnant women.

To date, we are not aware of any illnesses linked to this recall. Please see attached photos for further identification.

On 9/16/22 the firm was notified by their laboratory that a single sample of a product tested positive for Listeria monocytogenes.

Products affected are:

Product Name

Size

UPC

Sell-by Date

Lot Code

Asparagus Saute

9.5 oz

8 26766 19027 0

9/17/2022

GHGA 254

Diced Bell Pepper and White Onion

7 oz

8 26766 19004 1

9/15/2022

GHGA 254

Diced Red Onion

10 oz

8 26766 18100 1

9/19/2022

GHGA 254

Fajita Mix

9.5 oz

8 26766 19031 7

9/17/2022

GHGA 254

Fiesta Corn

10 oz

8 26766 18462 0

9/17/2022

GHGA 254

Hamburger Fixins

10 oz

8 26766 19028 7

9/17/2022

GHGA 254

Hatch Chile Guacamole Blender

9 oz

8 26766 14452 5

9/17/2022

GHGA 254

Large Medium Salsa

13 oz

8 26766 19071 3

9/18/2022

GHGA 254

Large Mild Chunky Guacamole

13 oz

8 26766 19053 9

9/17/2022

GHGA 254

Large Mild Salsa

13 oz

8 26766 19069 0

9/18/2022

GHGA 263

Mango Habanero Blender

9 oz

8 26766 19044 7

9/17/2022

GHGA 264

Medium Hatch Salsa

13 oz

8 26766 19076 8

9/18/2022

GHGA 265

Mexican Style Layered Bean Dip

20 oz

8 26766 14510 2

9/17/2022

GHGA 266

Mild Guacamole Blender

13 oz

8 26766 19045 4

9/17/2022

GHGA 267

Mild Guacamole Blender

9 oz

8 26766 14434 1

9/17/2022

GHGA 268

Mushroom Stir Fry Blend

9 oz

8 26766 19010 2

9/17/2022

GHGA 269

Seasoned Squash Onion & Dill

10.5 oz

8 26766 19036 2

9/17/2022

GHGA 270

Small Medium Hatch Chile Pico de Gallo

9 oz

8 26766 19062 1

9/18/2022

GHGA 271

Small Ranch Tray with Dip

21.0 oz

8 26766 19087 4

9/15/2022

GHGA 272

Snacking Peppers

12 oz

8 26766 19037 9

9/17/2022

GHGA 273

Spicy Guacamole Blender

9 oz

8 26766 14436 5

9/17/2022

GHGA 274

Steak Topper

7.5 oz

8 26766 19026 3

9/17/2022

GHGA 275

3 Skewer Veggie Kabobs

22 oz

8 26766 19008 9

9/17/2022

GHGA 276

Tri Pepper Blend

7 oz

8 26766 19003 4

9/15/2022

GHGA 277

Vegetable Bowl

42 oz

8 26766 18468 2

9/17/2022

GHGA 278

The products were sold to Kroger and distributed to retail stores on 9/11/22. The Sell-by Date has expired, and products were previously removed from store shelves and are no longer for sale. However, products could still be in possession of consumers. The Sell By Dates and Lot numbers are located on the top primary label of each product. These products were packaged in clear plastic containers and sold primarily in Kroger stores in the produce or deli sections in the states of: Alabama, South Carolina, and Georgia.

Consumers who have purchased these products are urged to return them to the place of purchase for a full refund or they may discard the product. Consumers with questions can call Customer Service at (888) 449-9386 M-F 8am – 4pm PST.

GHGA has notified Kroger and they have directed their stores to remove the products from the shelves.

This recall is being made with the knowledge of the Food and Drug Administration.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ghga-recalls-various-ready-eat-vegetable-products-due-possible-listeria-monocytogenes-contamination

Voluntary Recall of Certain Over-the-Counter Products Sold at Family Dollar Stores Because They Were Stored Outside of Temperature Requirements

September 16, 2022

More Information

Family Dollar is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and inadvertently shipped to certain stores on or around May 1, 2022 through June 10, 2022 due to product being stored outside of labeled temperature requirements. This notice covers the recall of Over-the-Counter Medical Devices. An earlier notice issued July 21, 2022 covered a related recall of Over-the-Counter Pharmaceutical Products.

To date, Family Dollar has not received any consumer complaints or reports of illness related to this recall. This recall is being conducted out of an abundance of caution.

A list of the recalled products is attached and below. This recall goes to the retail store level. Not all of the products listed were sent to all stores.

Family Dollar has notified its affected stores asking them to check their stock immediately and to quarantine and discontinue the sale of any affected product. Customers that may have bought affected product may return such product to the Family Dollar store where they were purchased without receipt. This recall does not apply to Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, Vermont, Washington, Alaska, or Hawaii as Family Dollar does not have any stores in Alaska or Hawaii and no Family Dollar stores in any of the other states received any products subject to this recall.

Customers with questions regarding this recall may contact Family Dollar Customer Service at 844-636-7687 between 9am and 5pm EST. Customers should contact their physician or health care 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
https://www.fda.gov/safety/report-problem-fda

Recalled Products

900260

900260 CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT

900794

900794 LS SKYN NON LATEX LUBRICATED CONDOM 3CT

901260

901260 VERIQUICK PREGNANCY TEST 1CT

902343

902343 FIRST RESPONSE 2 CT

903409

903409 SKYN ORIGINAL NON LATEX CONDOM 12CT

903415

903415 SKYN ELITE NON LATEX CONDOM 12CT

939504

939504 VERIQUICK PREGNANCY TEST 1 CT

900752

900752 AT HOME MARIJUANA TEST STRIP

902816

902816 TROJAN ULTRA RIBBED LUBED 3CT

903756

903756 VERIQUICK PREGNANCY TEST 2 CT

999763

999763 TROJAN ULTRA THIN CONDOM LATEX 3CT

998221

998221 SKYN ELITE LARGE NON LATEX CONDOM 12CT

998869

998869 PREFERRED UTI TEST 1 CT

900265

900265 LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT

900531

900531 CLEAR EYES CONTCT LENS DRPS LBRCTNG .5FO

999009

999009 B L BIOTRU MULTI PURPOSE SOLUTION 4 FLOZ

902274

902274 GS SALINE SOLUTION 12FL OZ

901443

901443 KY JELLY LUBRICANT 2 FL OZ

901960

901960 OPTI FREE REPLENISH MULTI PURPOSE 2 OZ

999801

999801 SIMPLY SALINE NASAL MIST 3.1 OZ

900457

OPTI FREE PURE MST DSINFCTNG SLTN 4FL OZ

902139

902139 DENTEMP ONE STEP .077OZ

906018

906018 FIXODENT ORG CREAM 2.4OZ

998762

998762 DRTALBOT TDDLR TTHPSTE BRSH TUTTI FRUTTI

905076

905076 CURAD STRNG WATRPRF STRIP 1IN 20CT

906312

906312 GS DENTURE CLEANSER GRN TAB 40CT

999619

999619 FIXODENT ADH CREAM ULTRA MAX HOLD 2.2OZ

999037

999037 CURAD FIRST AID KIT

903377

903377 POLIGRIP POWER MAX HOLD 2.2OZ

999417

999417 NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ

900737

900737 TRVL KIT TOTHBRSH CAP PASTE IN POUCH 1CT

901239

901239 FIXODENT ORG CREAM TRAVEL .75OZ

906131

906131 POLIDENT DENTURE CLNS TAB 28CT

900334

900334 POLIGRIP ADH CREAM FREE 2.4OZ

906023

906023 GS DENTURE CLEAN OVRNT TAB 40CT

901634

901634 POLIDENT DENTURE CLEANSERS 84 CT

901777

901777 POLIDENT OVERNIGHT WHITENING TAB 28CT

906402

906402 FIXODENT ADH CREAM WITH SCOPE 2OZ

999632

999632 POLIGRIP EXTRACARE ADHESIVE CREAM 2.2OZ

900085

900085 SUPER POLIGRIP ADH CREAM .75OZ

900723

900723 POLIGRIP DENTURE ADHESIVE ORIGINAL 2.4OZ

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-certain-over-counter-products-sold-family-dollar-stores-because-they-were-stored?utm_medium=email&utm_source=govdelivery

Valley International Cold Storage Acquisition, LLC, Recalls Frozen Beef Products Due To Misbranding And Undeclared Allergens

September 17, 2022

More Information

Valley International Cold Storage Acquisition, LLC, a Harlingen, Texas establishment, is recalling approximately 22,061 pounds of frozen beef products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains milk, a known allergen, which is not declared on the product label.

The frozen products are labeled as Korean-Style Beef, but contain a chicken sausage and pepper product, which contains milk. These items were produced on July 22, 2022. The following products are subject to recall [view labels]:

9.25-oz. cartons labeled as “Healthy Choice POWER BOWLS Korean-Style Beef” with lot code “5246220320” and a “best if used by” date of 04-18-2023.

The products subject to recall bear establishment number “34622” on the end flap of the carton. These items were shipped to retail locations nationwide.

The problem was discovered when the producing establishment notified FSIS that it had received consumer complaints that the Korean-Style Beef cartons contained a chicken-based 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. When available, the retail distribution lists will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers with questions about the recall can contact the Conagra Consumer Care line at 800-672-8152. Members of the media with questions about the recall can contact Daniel Hare, Senior Director of Communications, Conagra Brands, Inc., at 312-549-5355 or Daniel.Hare@conagra.com.

https://www.fsis.usda.gov/recalls-alerts/valley-international-cold-storage-acquisition-llc-recalls-frozen-beef-products-due

FSIS Issues Public Health Alert For Chicken Entree Products Due To Misbranding And An Undeclared Allergen

September 16, 2022

More Information

The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that the raw, ready-to-cook chicken entrée products may contain egg, a known allergen, which is not declared on the finished product label. FSIS is issuing this public health alert to ensure that consumers with an allergy to eggs are aware that these products should not be consumed. A recall was not requested because the products are no longer available for purchase.

The bacon-cheddar chicken entree products were produced on Sept. 9, 2022. The following products are subject to the public health alert [view labels]:

12 oz. plastic wrapped metal containers containing “aprons READY TO COOK MEAL FOR ONE BACON-CHEDDAR SMOTHERED CHICKEN” with a use by date of 9/21/2022.

The products bear establishment number “P-48176” inside the USDA mark of inspection. These items were shipped to Publix locations in Alabama, Florida, Georgia, North Carolina, South Carolina, Tennessee, and Virginia.

The problem was discovered when the establishment notified FSIS that they received notification from their customer that an incorrect label was on the back of the plastic wrapped metal container. The label on the back of the product contains information related to a chicken cordon bleu product, which does not contain egg. The bacon cheddar chicken product contains egg.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.

FSIS is concerned that some products may be in consumers’ refrigerators or freezers. Consumers with an egg allergy who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

Consumers and members of the media with questions about the public health alert can contact Diana Butz, Retail Compliance Manager of Tampa Bay Fisheries, at 813-752-8883, extension 208.

https://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-chicken-entree-products-due-misbranding-and

Muktan and Foods Inc. Issues an Allergy Alert on Ankur Brand Golden Raisin 14 Oz (400 GM)

September 13, 2022

More Information: “ANKUR” Muktan and Foods Inc. 483 Thomas Dr. Bensenville, IL 60106 is recalling its 14 Oz (400 gm) packages of “Golden Raisin” because they may contain undeclared sulfites. People who have severe sensitivity to Sulfites may run the risk of serious or life-threatening reactions, if they consume this product.

The product was sold in retail stores nationwide.

The product comes in 14 Oz, clear plastic package with UPC Code 8904 1704 10327. All ANKUR GOLDEN RAISIN 14Oz is impacted by this recall regardless of the presence or absence of a batch number.

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

The recall was initiated immediately after it was discovered that product was distributed in packaging that did not reveal the presence of Sulfite.

Consumers who have purchased 14 Oz packet of “Ankur Golden Raisin” are urged to return them to the place of purchase for a full refund.

Consumers with question may call Raxa Desai at 630-595-1118 Monday to Friday 9 am to 5 pm CST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/muktanand-foods-inc-issues-allergy-alert-ankur-brand-golden-raisin-14-oz-400-gm

FSIS Issues Public Health Alert For Specific Ground Beef In HelloFresh Meal Kits Due to Possible E. Coli O157:H7 Contamination

September 10, 2022

More Information

The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert due to concerns that ground beef products in HelloFresh meal kits may be associated with Escherichia coli (E. coli) O157:H7 illness. A recall was not requested because the products are no longer available for purchase.

The meal kits containing ground beef for this public health alert were shipped to consumers from July 2-21, 2022. The following products are subject to the public health alert [view label]:

10-oz. plastic vacuum-packed packages containing “GROUND BEEF 85% LEAN/15% FAT” with codes “EST#46481 L1 22 155” or “EST#46481 L5 22 155” on the side of the packaging.

The ground beef packages bear “EST.46841” inside the USDA mark of inspection and on the plastic ground beef package.

FSIS, the Centers for Disease Control and Prevention, and state public health partners are investigating an outbreak of E. coli O157:H7 and raw ground beef is the probable source of the reported illnesses. Traceback information identified that multiple case-patients received ground beef produced at establishment M46841 and distributed by HelloFresh in meal kits from July 2-21, 2022. Traceback of materials used to produce the ground beef is ongoing and FSIS continues to work with suppliers and public health partners on the investigation.

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.

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.

Media and consumers with questions regarding the public health alert can contact hello@hellofresh.com or by live chat.

https://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-specific-ground-beef-hellofresh-meal-kits-due

Sunset Farm Foods Inc., Recalls Sausage Products Due to Possible Foreign Matter Contamination

September 7, 2022

More Information

Sunset Farm Foods Inc., a Valdosta, Ga. establishment, is recalling approximately 4,480 pounds of chicken and pork smoked sausage products that may be contaminated with extraneous materials, specifically thin blue plastic, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The fully cooked chicken and pork smoked sausage items were produced on June 30, 2022. The following products are subject to recall [view labels]:

28-oz. vacuum sealed packages of “Georgia Special Chicken and Pork Smoked Sausage” with a sell by date of 10-28-22.

The products subject to recall bear establishment number “P 9185” inside the USDA mark of inspection. These items were shipped to retail locations in Alabama, Florida, Georgia, and North Carolina.

The problem was discovered when the establishment reported to FSIS that it received consumer complaints reporting thin blue plastic embedded inside the pork and chicken sausage product.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

FSIS is concerned that some product may be in consumers’ refrigerators or freezers. 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 Russell Harris, Quality Assurance Manager of Sunset Farm Foods Inc., at 229-242-2952 or by email at R.Harris@sunsetfarmfoods.com. Members of the media with questions about the recall can contact Tom Carroll, Owner/President of Sunset Farm Foods Inc., at 229-242-2952 or by email at T.Carroll@sunsetfarmfoods.com.

https://www.fsis.usda.gov/recalls-alerts/sunset-farm-foods-inc--recalls-sausage-products-due-possible-foreign-matter

Magnolia Provision Company, Inc., Recalls Beef Jerky Products Due to Possible Listeria Contamination

September 6, 2022

More Information

Magnolia Provision Company, Inc., a Knoxville, Tenn. establishment, is recalling approximately 497 pounds of beef jerky products that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The ready-to-eat beef jerky items were produced on August 25, 2022. The following products are subject to recall [view labels]:

2-oz. packages of “BEEF JERKY EXPERIENCE CHOP HOUSE STYLE PRIME RIB FLAVORED BEEF JERKY” with “EXP 8/25/23” displayed on the back of the package.
8-oz. packages of “BEEF JERKY EXPERIENCE CHOP HOUSE STYLE PRIME RIB FLAVORED BEEF JERKY” with “EXP 8/25/23” displayed on the back of the package.
16-oz. packages of “BEEF JERKY EXPERIENCE CHOP HOUSE STYLE PRIME RIB FLAVORED BEEF JERKY” with “EXP 8/25/23” displayed on the back of the package.

The products subject to recall bear establishment number “EST. 8091” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.

The problem was discovered when the establishment reported to FSIS that it received confirmation from their third-party lab that a product contact surface sample returned as positive for Listeria monocytogenes.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.

Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.

FSIS is concerned that some product may be in consumers’ 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 recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Media and consumers with questions regarding the recall can contact Rob Noyes, Vice President of Magnolia Provision Company, Inc., at Rob@magnoliajerky.com.

https://www.fsis.usda.gov/recalls-alerts/magnolia-provision-company-inc--recalls-beef-jerky-products-due-possible-listeria

St. James Smokehouse Voluntary Recalls Scotch Reserve Scottish Smoked Salmon 4oz (Lot# 123172) Because Of Possible Health Risk

September 2, 2022

More Information: St. James Smokehouse of Miami, Florida is voluntary recalling 93 cases of St. James Smokehouse brand, Scotch Reserve Scottish Smoked Salmon, 4oz Packages (Product of Scotland) because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

The recalled product was sold and distributed by St. James via distributors between February and June 2022. The recalled product was distributed to stores located in: Alabama, Colorado, Florida, Illinois, New Jersey, New York, Massachusetts, Washington State, Virginia and Wisconsin as well as Safeway Washington State stores.

The recalled product is St. James Scotch Reserve Scottish Smoked Salmon (Product of Scotland), 4oz packages, bearing the lot# 123172 and UPC code 060022710356. The recall is specifically this lot ONLY, NO other products, brands or lots are associated with this recall.

If consumers have products matching the above description and lot# in their possession, they should dispose of it immediately or return it to the store for a full refund.

As of Friday, September 2, 2022 no illnesses have been reported.

The recall was the result of a routine sampling by the Washington State Department of Agriculture which revealed that the finished product contained the bacteria.

This voluntary recall is being conducted in cooperation with the U.S. Food and Drug Administration.

Consumers that may have any questions about the recall may call 305-461-0231, Monday through Friday from 8:00am – 5:00 pm EST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/st-james-smokehouse-voluntary-recalls-scotch-reserve-scottish-smoked-salmon-4oz-lot-123172-because?utm_medium=email&utm_source=govdelivery

Food Co. Issues Allergy Alert on Undeclared Coconut in Product

September 1, 2022

More Information: Toufayan Bakery is voluntarily recalling Publix GreenWise Animal Crackers with a UPC of 0-41415-12009-9. (Located on the back of the pouch) and with an expiration date of Feb 05, 2023 due to an undeclared tree nut allergen. The cookies are packaged in pouches, net weight 8 oz and may contain coconut. People who have an allergy or severe sensitivity to tree nuts run the risk of serious or life-threatening allergic reaction if they consume this product. Product was distributed to Publix Supermarkets in Florida, Alabama, Georgia, South Carolina, North Carolina, Virginia and Tennessee.

Subsequent investigation indicates the problem was caused by a temporary breakdown in the production and packaging processes.

Customers who have purchased Publix GreenWise Animal Crackers are urged to return it to their local store for a full refund

Consumers with questions may contact the Toufayan at 1-813-754-5565

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/food-co-issues-allergy-alert-undeclared-coconut-product?utm_medium=email&utm_source=govdelivery

Albertsons Companies Expands Voluntary Recall of Select ReadyMeals Seafood Products Due to Undeclared Allergens

August 31, 2022

More Information

Albertsons Companies today announced it is expanding its July 19, 2022, voluntary recall of ReadyMeals seafood items due to allergens not listed on the ingredient labels. The recall, which is being conducted in continued collaboration with the U.S. Food and Drug Administration, was initiated after an internal technical review identified missing ingredients containing allergens.

Consumers who have certain food allergies or severe sensitivities run the risk of serious or life - threatening allergic reactions if they consume these products and are urged not to consume these items. These consumers should discard the products or return them to their local store for a full refund.

There have been no reports of injuries or adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

The two select ReadyMeals seafood items were available for purchase at the following Albertsons Cos. store banners: Safeway and Albertsons located in Oregon and select cities in Washington state (Battle Ground, Camas, Hazel Dell, Kelso, Longview, Vancouver, Walla Walla, Washougal and Woodland).

Consumers with questions should contact Albertsons Cos. Customer Service Center at 1-877-723-3929 for additional information Monday through Friday from 5 a.m. to 9 p.m. PST.

Product Recall Details:

Product Name

Size

Undeclared Allergens

Packaging

UPC

Sell Thru Dates

Store Banners

States

ReadyMeals Shrimp Cooked with Cocktail Sauce

12 oz

Fish (Anchovy)

Clear plastic container with four compartments

23463800000

All Sell Thru Dates up to and including Sept. 1

Albertsons, Safeway

OR, WA

ReadyMeals Snow Crab Legs Imitation Surimi

12 oz

Fish (Anchovy)

Clear plastic container with four compartments

23463900000

All Sell Thru Dates up to and including Sept. 1

Albertsons, Safeway

OR, WA

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/albertsons-companies-expands-voluntary-recall-select-readymeals-seafood-products-due-undeclared?utm_medium=email&utm_source=govdelivery

Keswick Creamery at Carrock Farm, LLC Recalls Cheese Because of Possible Health Risk

August 29, 2022

More Information

Keswick Creamery of Newburg, Pa is recalling Calverley Cheese, Vulkwin’s Folly Cheese, Vermeer Cheese, Havarti Cheese, Wallaby Cheese, Cider Washed Tomme Cheese, Feta Cheese, Whole Milk Ricotta, Bovre Cheese (plain, oregano and garlic, herbes de provence, cranberry and honey) and Quark Cheese (plain, dill and onion), because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

All Cheeses were distributed at Dupont Circle Freshfarm Market in Washington, D.C.; Takoma Park Farmers Market in Takoma Park, Maryland; Smith Meadows Farm Store in Berryville, Virginia; Oylers Organic Farms and Market in Biglerville, Pennsylvania; and Talking Breads Farm Store in Mechanicsburg, Pennsylvania.

The cheeses will be labeled from Keswick Creamery, with the cheese name on the label.

Calverley Cheese in 4 oz to 12 oz packages, price and weight labeled in red, black, or purple ink
Vulkwin’s Folly Cheese in 4 oz to 12 oz packages, price and weight labeled in red, black, or purple ink
Havarti Cheese in 4 oz to 12 oz packages, price and weight labeled in red, black, or purple ink
Vermeer Cheese in 4 oz to 12 oz packages, price and weight labeled in red, black, or purple ink
Wallaby Cheese in 4 oz to 12 oz packages, price and weight labeled in red, black, or purple ink
Cider Washed Tomme Cheese in 4 oz to 12 oz packages, price and weight labeled in red, black, or purple ink
Feta cheese in 4 oz to 12 oz packages, price and weight labeled in red, black, or purple ink
Whole Milk Ricotta, 8 oz and 16 oz clear deli container, expiration dates 7/18/22, 7/25/22, 8/1/22, 8/8/22, 8/18/22
Bovre Cheese (plain, oregano and garlic, herbes de Provence, cranberry and honey), 8oz clear deli container, expiration dates 7/25/22, 8/1/22, 8/8/22, 8/22/22
Quark Cheese (plain and dill and onion), 8 oz and 16 oz clear deli container, expiration dates 7/7/22, 8/4/22, 8/25/22

No illnesses have been reported to date.

The recall was the result of a routine sampling program conducted by the FDA which revealed some finished products contained the bacteria. Keswick Creamery has ceased the production and distribution of all products as FDA and the company continue their investigation as to what caused the problem.

Consumers who have purchased any of the listed cheese from Keswick Creamery at Carrock Farm, LLC are urged to discard the product. Customers should email Keswick Creamery directly at keswickrecall@gmail.com or call 1-800-946-1631 Monday thru Friday 10 am to 2 pm Eastern time to report their product and receive a full refund.

Keswick Creamery at Carrock Farm, LLC
114 Lesher Road
Newburg, Pa 17240

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/keswick-creamery-carrock-farm-llc-recalls-cheese-because-possible-health-risk?utm_medium=email&utm_source=govdelivery

Tai Phat Wholesalers, LLC Recalls “Three Coins Dried Mushrooms” Because of Possible Health Risk

August 30, 2022

More Information

Tai Phat Wholesalers, LLC of Capitol Heights, MD is recalling 4 types of packages of its “Three Coins Dried Mushrooms” because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

The recalled Dried Mushrooms were distributed in specialty retail stores in the following states: Florida, Georgia, Kentucky, Maryland, Massachusetts, Minnesota, Mississippi, New Hampshire, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, Tennessee, Virginia.

The product comes in four different types & sizes and are in a sealed clear plastic package with a label. The different types are as follows:

Three Coins Dried Mushrooms Slices – Item #: 01051- Nam Meo Soi -S- 2.5 oz
Three Coins Dried Mushrooms Slices – Item #: 01276- Nam Meo Soi -L- 10.5 oz
Three Coins Dried Mushrooms Whole – Item #: 01052- Nam Meo Nguyen -S- 2.5 oz
Three Coins Dried Mushrooms Whole – Item #: 01277- Nam Meo Nguyen -L- 10.5 oz

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

The potential for contamination was noted after routine testing by Maryland Department of Health of items bought at a retail store which revealed the presence of Salmonella in some packages of "Three Coins Dried Mushrooms".

Sales of the product has been suspended while MDH and the company continue their investigation as to the source of the problem.

Consumers who have purchased the packages of "Three Coins Dried Mushrooms" are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-703-538-8000.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tai-phat-wholesalers-llc-recalls-three-coins-dried-mushrooms-because-possible-health-risk?utm_medium=email&utm_source=govdelivery

Valrhona Inc. Recalls Ineligible Egg Products Produced In Italy

August 31, 2022

More Information

Valrhona Inc., a Brooklyn, New York establishment, is recalling approximately 66 pounds of dried albumin egg products, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products were produced in Italy, a country ineligible to export egg products to the United States.

The dried albumin egg products were produced on Feb. 2, 2022, March 18, 2022, June 17, 2022, and July 19, 2022. The following products are subject to recall [view labels]:

1.1-lb. plastic canister containing “Sosa ALBUWHIP” with lot code LALB22033, LALB22077, LALB22168 or LALB22200.

These items were shipped to locations in California, Florida, Nevada, and New York.

The problem was discovered when FSIS investigated and determined that the egg products were produced in Italy, a country ineligible to export egg products to the United States.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS is concerned that some product may be in consumers’ pantries or in restaurants. Consumers who have purchased these products are urged not to consume them. Restaurants and institutions are urged not to serve these products. 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 Ms. Raphaele Bonnaure, Director of Supply Chain, Valrhona Inc. at (929) 884-9600 or raphaele.bonnaure@valrhona.fr.

https://www.fsis.usda.gov/recalls-alerts/valrhona-inc--recalls-ineligible-egg-products-produced-italy

Connoisseur’s Kitchen Recalls Imported Frozen Chicken Products Due to Possible Listeria Contamination

August 30, 2022

More Information

Connoisseur’s Kitchen, a Surrey, British Columbia establishment, is recalling approximately 880 pounds of frozen ready-to-eat (RTE) chicken entree products that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The frozen RTE chicken entree items were produced on Aug. 3, 2022 and imported to the U.S. on Aug. 8, 2022. The following products are subject to recall [view labels]:

2-lb. box packages containing “SPICE MANTRA CHICKEN KORMA” with lot code 220803-406US.
2-lb. box packages containing “SPICE MANTRA BUTTER CHICKEN” with lot code 220803-400US.

The products subject to recall bear establishment number “780” inside the Canadian mark of inspection. These items were shipped to retail locations in Alaska and Washington.

The problem was discovered when the Canadian Food Inspection Agency notified FSIS that the products are associated with a sample that tested positive for Listeria monocytogenes.

There have been no confirmed reports of illness or adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.

Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.

FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Media and consumers with questions regarding the recall can contact Puneet Bhalla, Director for Connoisseur’s Kitchens, at (604) 595-4862, ext. 25.

https://www.fsis.usda.gov/recalls-alerts/connoisseurs-kitchen-recalls-imported-frozen-chicken-products-due-possible-listeria

Van Law Food Products Issues Allergy Alert on Undeclared Soy and Wheat in Product

August 26, 2022

More Information: Van Law Food Products Inc. is recalling Whole Foods Market 365 Organic Creamy Caesar Dressing because it contains undeclared Soy and Wheat allergens.

People with an allergy or severe sensitivity to Soy or Wheat run the risk of serious or life-threatening allergic reaction if they consume these Ingredients. The product was sold in the produce or dairy department and distributed in the states of Alabama, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New Jersey, New Mexico, New York, North Carolina, Ohio, South Carolina, Tennessee, Texas, Utah, Wisconsin, and Wyoming.

No illnesses have been reported to date.

The recall was initiated after it was discovered that the product was distributed in packaging that did not reveal the presence of Soy and Wheat allergen. Subsequent investigation indicates that the problem was caused when the back label from another product was mistakenly put on the product being recalled.

Consumers who purchased Whole Foods Market 365 Organic Creamy Caesar Dressing with UPC code 99482-49027 in 12oz glass bottles with a Best by date of 04/06/2023 should discard the product and seek a refund at the point of sale with receipt. Consumers with additional questions can call 1- 844-936-8255 between the hours of 7:00 am and 10:00 pm CST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/van-law-food-products-issues-allergy-alert-undeclared-soy-and-wheat-product?utm_medium=email&utm_source=govdelivery

D.F. Stauffer Biscuit Co., Inc. Issues a Voluntary Recall on Market Pantry White Fudge Animal Cookies with a Best By Date of 21FEB2023 Due to Possible Foreign Object Contamination

August 25, 2022

More Information

D. F. Stauffer Biscuit Co., Inc. is voluntarily recalling 44 oz Market Pantry White Fudge Animal Cookies because they may contain metal. The product comes in a clear plastic jug formed to a bear shape. The recall affects only the following Best By Date, Lot Numbers, and time stamps, printed on the back side of the bear jug on the product label, below the nutritional panel.

Best by Date

Jug Lot Numbers

Case Lot Number

Time Stamp

UPC Code

21FEB2023

Y052722

From 15:00 to 23:00

085239817698

The products were distributed to Target stores nationwide. No other lots or products are affected.

The recall was initiated when metal (wire) was found inside a portion of the cookies. Foodborne foreign objects that are hard, sharp, and large are more likely to cause serious injury or dental injury. Foodborne foreign objects that are flexible, not sharp, and smaller in length are more likely to cause minor injuries such as transient choking or small lacerations in the gastrointestinal system.

Consumers who have purchased the recalled product are urged to stop consuming the product and return it to the place of purchase for a full refund. Consumers with questions may contact D.F. Stauffer Biscuit Co., Inc. at 888-480-1988, Mon-Fri, 8am to 5pm EST.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/df-stauffer-biscuit-co-inc-issues-voluntary-recall-market-pantry-white-fudge-animal-cookies-best?utm_medium=email&utm_source=govdelivery

Piantedosi Baking Company, Inc. Issues Voluntary Recall Due to the Recall of a Raw Material from Lyons Magnus

August 25, 2022

More Information

Out of an abundance of caution, Piantedosi Baking Company, Inc. is voluntarily recalling select dinner rolls, sandwich rolls and bun products listed below that were used in limited products made between March 21,2022 and April 25, 2022, following the expanded Lyons Magnus recall dated August 10, 2022 recall of a raw material (FDA publish date August 16, 2022), used in limited production of dinner rolls, sandwich rolls and bun products from the manufacturer of Golden Gloss glaze (Lyons Magnus). Lyons Magnus is recalling this raw material due to the potential for it to cause microbial contamination, including the organisms Cronobacter sakazakii and/or Clostridium botulinum. While no illnesses associated with Piantedosi Baking Company, Inc. bread products have been reported and no pathogens have been found in Piantedosi Baking Company, Inc. products to date, this voluntary recall is being conducted out of an abundance of caution to ensure customer safety.

This recall does not impact any other Piantedosi Baking Company, Inc. products, as no other products were produced with this raw material from Lyons Magnus.

We advise that distributors and end users in possession of any of these Piantedosi dinner rolls, sandwich rolls and/or buns immediately examine your inventory for any of the affected lot codes and place any remaining products you may have on hold. Cease further distribution of these affected products, and do not consume these affected products. Distributors and/or end users in possession of any of the affected product lots listed should contact your Piantedosi Baking Company, Inc. representative to coordinate return of the product and for replacement of product. In the event you do not have any of the affected lot codes in your inventory, please retain this notice in the event any of your customers and/or end users have any questions.

We advise that in the event any consumers are in possession of any of these affected Piantedosi dinner rolls, sandwich rolls and/or buns should dispose of the product. Consumers can contact Piantedosi Baking Company, Inc. at 800-339-0080 x165, Monday through Friday from 10:00 a.m. to 4:00pm ET, if they have any questions, or to request replacement product.

The affected lots of Golden Gloss glaze received were used for a limited production period between March 21, 2022 and April 25, 2022. See below for the list of the affected Piantedosi Baking Company product UPC #s and lot codes.

Cased SKU #

Cased Product Name

Case Count

UPC

Lot Codes

Expiration Date

C-88

Finger Roll

24-pk/
192 count

033474400885

22082
22096
22102
22109

3/23/2023
4/6/2023
4/12/2023
4/19/2023

C-96

Soft Dinner Roll No Seeds

24-pk/
192 count

033474400960

22082
22091
22096
22103
22110

3/23/2023
4/1/2023
4/6/2023
4/13/2023
4/20/2023

C-130-S

Gourmet Junior Burger Roll

12-pk/
120 count

033474501308

22083
22104
22112
22115

3/24/2023
4/14/2023
4/22/2023
4/25/2023

C-132

Gourmet Burger Roll

12-pk/
96 count

033474501322

22083
22088
22091
22095
22101
22105
22109
22112

3/24/2023
3/29/2023
4/1/2023
4/5/2023
4/11/2023
4/15/2023
4/19/2023
4/22/2023

C-133

SPR Roll

12-pk/
96 count

033474501339

22083
22084
22087
22094
22102
22104
22108
22111
22112
22115

3/24/2023
3/25/2023
3/28/2023
4/4/2023
4/12/2023
4/14/2023
4/18/2023
4/21/2023
4/22/2023
4/25/2023

C-136

Seeded SPR Roll

12-pk/
96 count

033474501360

22084
22098
22105
22112

3/25/2023
4/8/2023
4/15/2023
4/22/2023

C-285

Clustered Potato Burger Roll

12-pk/
96 count

033474502855

22105
22112

4/15/2023
4/22/2023

C-294-S

B & W Sweet Burger Roll

12-pk/
96 count

033474502947

22092
22099

4/2/2023
4/9/2023

C-297-S

Hawaiian Sandwich Roll

12-pk/
96 count

033474502978

22110

4/20/2023

C-364

Gourmet Potato Deli Roll

12-pk/
96 count

033474503647

22081
22084
22094
22101
22102
22108
22110
22111
22115

3/22/2023
3/25/2023
4/4/2023
4/11/2023
4/12/2023
4/18/2023
4/20/2023
4/21/2023
4/25/2023

C-377-S

Split Top Burger Roll

12-pk/
96 count

033474503777

22081
22094

3/22/2023
4/4/2023

C-417-S

Brioche Style Burger Roll

12-pk/
96 count

033474504170

22082
22095
22103
22109

3/23/2023
4/5/2023
4/13/2023
4/19/2023

C-418-S

Sunset Burger Roll

12-pk/
96 count

033474504187

22104
22110

4/14/2023
4/20/2023

C-464-S

B & W Gourmet Burger Roll

12-pk/
96 count

033474504644

22085
22092
22106
22112

3/26/2023
4/2/2023
4/16/2023
4/22/2023

C-494-S

Slider Rolls No Seeds

24-pk/
192 count

033474504941

22082
22096
22103
22110

3/23/2023
4/6/2023
4/13/2023
4/20/2023

C-952

Gourmet Potato Deli Roll

8-pk/
96 count

033474509526

22094
22102

4/4/2023
4/12/2023

C-1202-S

Brioche-Style Slider Roll

24-pk/
192 count

033474512021

22081
22088
22095
22102
22109

3/22/2023
3/29/2023
4/5/2023
4/12/2023
4/19/2023

C-1204-S

Gourmet Potato Slider Rolls

24-pk/
192 count

033474512045

22081
22088
22091
22095
22102
22103
22104
22105
22110

3/22/2023
3/29/2023
4/1/2023
4/5/2023
4/12/2023
4/13/2023
4/14/2023
4/15/2023
4/20/2023

Below is the list of affected Piantedosi Baking Company, Inc. tray products which have expired and should no longer be in the marketplace:

Tray SKU #

Tray Product Name

Pack Size

UPC

Lot Codes

Expiration Date

#14 & #16

Soft Dinner Rolls with No Seeds

12 & 24-pack

033474000146

22081
22096
22102
22103
22109
22110

3/29/2022
4/13/2022
4/19/2022
4/20/2022
4/26/2022
4/27/2022

#20

Finger Roll

24-pack

033474000207

22082
22096
22102
22109

3/30/2022
4/13/2022
4/19/2022
4/26/2022

#132-TR

Gourmet Burger Roll

12-pack

033474501322

22094
22101

4/14/2022
4/21/2022

#133-STR

SPR Roll

12-pack

033474501339

22083
22084
22087
22094
22102
22104
22108
22111
22112
22115

4/7/2022
4/8/2022
4/11/2022
4/18/2022
4/26/2022
4/28/2022
5/2/2022
5/5/2022
5/6/2022
5/9/2022

#283-TR

Jr. Potato Burger Roll

8-pack

033474502831

22083
22088
22108

3/31/2022
4/5/2022
4/25/2022

#285TR

Clustered Potato Burger Roll

12-pack

033474502855

22105
22112

4/22/2022
4/29/2022

#364-TR

Gourmet Potato Deli Roll

12-pack

033474503647

22081
22084
22094
22101
22102
22108
22110
22111
22115

3/29/22
4/1/2022
4/11/2022
4/18/2022
4/19/2022
4/25/2022
4/27/2022
4/28/2022
5/2/2022

#416-STR

Sweet Potato Sandwich Roll

12-pack

033474504163

22095
22105
22110

4/15/2022
4/25/2022
4/30/2022

#417-STR

Brioche Style Burger Roll

12-pack

033474504170

22082
22083
22088
22091
22095
22101
22105
22109
22110

4/2/2022
4/3/2022
4/8/2022
4/11/2022
4/15/2022
4/21/2022
4/25/2022
4/29/2022
4/30/2022

#464-STR

B & W Gourmet Burger Roll

12-pack

033474104646

22085
22092
22106
22112

4/2/2022
4/9/2022
4/23/2022
4/29/2022

#1202-TR

Brioche-Style Slider Roll

24-pack

033474512021

22081
22088
22095
22102
22109

3/29/2022
4/5/2022
4/12/2022
4/19/2022
4/26/2022

#1204-STR

Gourmet Potato Slider Rolls

24-pack

033474512045

22081
22088
22091
22095
22102
22103
22104
22105
22110

3/29/2022
4/5/2022
4/8/2022
4/12/2022
4/19/2022
4/20/2022
4/21/2022
4/22/2022
4/27/2022

#1297-TR

Garlic & Herb Dinner Roll

12-pack

033474012972

22082

4/5/2022

#6457-TR

Sweet Potato Dinner Roll

12-pack

033474010473

22082
22088
22096
22102

4/5/2022
4/11/2022
4/19/2022
4/25/2022

#6458-TR

Potato Slider Roll

12-pack

033474510546

22082
22088
22102
22110

4/5/2022
4/11/2022
4/25/2022
5/3/2022

#6462-TR

Potato Finger Roll

12-pack

033474011296

22082
22096
22102
22109

4/5/2022
4/19/2022
4/25/2022
5/2/2022

#6467-TR

Brioche-Style Bulkie Rolls

6-pack

075199017245

22080
22083
22087
22094
22101
22104
22108
22111

4/3/2022
4/6/2022
4/10/2022
4/17/2022
4/24/2022
4/27/2022
5/1/2022
5/4/2022

#6470-TR

Onion Bulkie Roll

6-pack

075199001329

22080
22083
22087
22094
22095
22101
22104
22108
22109
22111

4/3/2022
4/6/2022
4/10/2022
4/17/2022
4/18/2022
4/24/2022
4/27/2022
5/1/2022
5/2/2022
5/4/2022

#6481-TR

Potato Hamburger Roll

8-pack

075199064812

22087
22095
22101
22104
22108
22111

4/10/2022
4/18/2022
4/24/2022
4/27/2022
5/1/2022
5/4/2022

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/piantedosi-baking-company-inc-issues-voluntary-recall-due-recall-raw-material-lyons-magnus?utm_medium=email&utm_source=govdelivery

Pizza John’s Recalls Pepperoni Pizza Products Produced Without Benefit of Inspection

August 25, 2022

More Information

Pizza John’s, an Essex, Md. firm, is recalling approximately 156,498 pounds of pepperoni pizza 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 pepperoni pizza products were produced and distributed into commerce on dates from March 2020 through July 28, 2022. The following products are subject to recall [view labels]:

33.25-oz. clear plastic wrapped packages containing “PIZZA JOHN’S BAKE AT HOME 12 Inch Pepperoni Pizza” with UPC code 9589334921.
57-oz. clear plastic wrapped packages containing “PIZZA JOHN’S BAKE AT HOME 16 Inch Pepperoni Pizza” with UPC code 958939019.

The products subject to recall do not bear the USDA mark of inspection because Pizza John’s is not a federally inspected establishment. These items were shipped to retail locations in Maryland.

The problem was discovered during routine FSIS surveillance activities when it was determined that the pepperoni pizza products did not have the USDA mark of inspection and were produced in an establishment that was not inspected by USDA.

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 Melissa Steall, Office Manager, Pizza John’s, at 410-687-1155.

https://www.fsis.usda.gov/recalls-alerts/pizza-johns-recalls-pepperoni-pizza-products-produced-without-benefit-inspection

South Georgia Pecan Co. Recalls Great Value 4oz. Walnut Chopped Pouches Due to Pouch Containing Pecan Pieces

August 23, 2022

More Information

South Georgia Pecan Co. is recalling Great Value Walnut Chopped 4oz. Pouches Lot #29329 Best If Used By April 29, 2023 due to pouches containing pecan pieces instead of walnuts. This recall has been initiated due to mislabeling issue where a packaging run of pecans was labeled as Chopped Walnuts. People who have an allergy or severe sensitivity to pecans run the risk of serious or life-threatening allergic reaction if they consume this product. See enclosed product label to help in identifying the product at retail/user level.

No illnesses have been reported to date.

Products affected are:

Product

Size

Lot #

UPC

Use By Dates

Great Value Walnut Chopped Pieces

4 oz. Reseable Pouch

29329

78742201344

April 29, 2023

On 8/16/2022 the firm was notified by retailer that Great Value 4oz. Walnut Chopped Pouches contained pecan pieces. The product was distributed between August 8, 2022 – August 16, 2022. This product was packaged in resealable pouches and shipped to select Walmart retail stores located in the States of: Florida, North Carolina, and South Carolina.

Consumers who have purchased these products are urged to return them to the place of purchase for a full refund or they may discard the product. Consumers with questions may contact Customer Service at 1-800-627-6630; Monday – Friday 08:00am – 5:00pm ET.

This recall is being made with the knowledge of the Food and Drug Administration.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/south-georgia-pecan-co-recalls-great-value-4oz-walnut-chopped-pouches-due-pouch-containing-pecan?utm_medium=email&utm_source=govdelivery

Rushdi Foods Issues a Voluntary Recall on One Lot of their Mighty Sesame Organic Tahini 10.9 oz Squeeze Bottle

August 23, 2022

More Information

Rushdi Food Industries, an Israeli based manufacturer, is voluntarily recalling their Mighty Sesame 10.9 Oz Organic Tahini (Squeezable) with the specific expiration date of 3/28/23 due t0 potential Salmonella contamination. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (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 severs illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

This recall was initiated when the company received a notification by the FDA and the West Virginia Department of Health of the potential presence of Salmonella in this specific lot. The company has received no reports of illness or injury to date. We immediately informed all Stores who had purchased this product within this lot code about this Recall and instructed them to remove any product which might be on their shelves. The Facility reviewed cleaning procedures, Environmental Monitoring Program Results, Process Flow and possible Root of Contamination without any positive findings.

Only packages bearing the following Lot Code/Best by date are being recalled at this time. All products other than the ones with the affected Best by Date mentioned in the table are ok to consume.

UPC Code

Description

Expiration Date

858313006208

Mighty Sesame 10.9 Oz Organic Tahini (Squeezable)

3/28/23

The recalled product was distributed to stores located in the New York, New Jersey and Connecticut as well as Wal-Mart stores nationwide during the first 2 weeks of May 2022. Based off of sales velocity, there is an extremely low chance that any of the affected product would still be available for retail. All products other than the ones with the affected Best by Date mentioned in the table are ok to consume.

Consumers who may have purchased this product are advised to discontinue use immediately and discard or return the product for credit or refund. If a consumer experiences the symptoms listed above and believes they may have been exposed to Salmonella, they are urged to report to a medical provider.

Consumers who have questions may contact us at Customercare@kayco.com or by phone at 718-369-4600 Monday through Friday 9 AM to 5PM Eastern Time.

This recall is being made with the knowledge of the Food and Drug Administration.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/rushdi-foods-issues-voluntary-recall-one-lot-their-mighty-sesame-organic-tahini-109-oz-squeeze?utm_medium=email&utm_source=govdelivery

FSIS Issues Public Health Alert for Perdue Frozen Ready-To-Eat Chicken Tender Products Due to Foreign Material Contamination

August 23, 2022

More Information

The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for Perdue’s frozen ready-to-eat (RTE) chicken breast tenders “gluten free” that may be contaminated with extraneous materials, specifically small pieces of clear plastic and blue dye. A recall was not requested because the product is no longer available for purchase.

The frozen RTE chicken breast tenders “gluten free” were produced on July 12, 2022. The following product is subject to the public health alert [view labels]:

42 oz. plastic bags containing “PERDUE CHICKEN BREAST TENDERS GLUTEN FREE” with a “Best if Used By: 07 12 23” and a lot number of 2193 above the use by date.

The products bear establishment number “P-33944” immediately below the “Best if Used By:” date on the back of the plastic bag. These items were shipped to BJ's Wholesale Club retail locations nationwide.

The problem was discovered when the establishment reported to FSIS that it received a complaint from a consumer reporting a chicken tender had a small piece of clear plastic and blue dye inside it.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.

FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

Members of the media with questions about the public health alert can contact Andrea Staub, Senior Vice President of Perdue Foods LLC, at 410-341-2755 or by email at andrea.staub@perdue.com. Consumers with questions may call the Perdue Foods LLC hotline at 866-866-3703.

https://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-perdue-frozen-ready-eat-chicken-tender-products-due

Epicurean Butter Recalls “Wegmans Lemon Dill Finishing Butter” Because of Possible Health Risk

August 19, 2022

More Information

Epicurean Butter LLC of Thornton, CO, is recalling its 3.5-ounce tubs of " Wegmans Lemon Dill Finishing Butter" food due to a recall from our frozen dill supplier, SupHerb Farms, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

The recalled "Wegmans Lemon Dill Finishing Butter " were distributed at Wegmans Food Markets in New York, Pennsylvania, New Jersey, Maryland, Massachusetts, Virginia, North Carolina, and Washington DC.

The product comes in a 3.5-ounce, black plastic cup with a Wegmans label around and on the lid. The cup has a sealed lidding film under the lid. There is a “Best By” and Lot # printed with blue ink by the label around the cup. The following products are subject to this recall.

Product Name

Item #

UPC Code

Lot #

Expiration Date

Qty