Current Recalls

Champion Foods Recalls Some Batches of 5 Cheese Bread MAY 29, 2026 – Champion Foods LLC of New Boston, Michigan, is voluntarily recalling certain batches of Motor City Pizza Co. 5 Cheese Bread because they have the potential to be contaminated with Salmonella. This action follows a California Dairies, Inc. milk powder recall due to a concern of potential Salmonella contamination. Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e. infected aneurysms), endocarditis, and arthritis.The recalled milk powder was supplied to a third-party manufacturer that provides a seasoning blend used in our 5 cheese sauce blend. To date, neither Champion Foods LLC nor our suppliers have received any reports of illness or injury related to these products. Routine testing conducted by the seasonings blend manufacturer prior to use in the production of the 5 Cheese Bread showed that the seasonings batches tested negative for Salmonella; however, we are taking action out of an abundance of caution for the safety of our customers. Affected 5 Cheese Bread lots were distributed and sold nationwide at retailers including Costco, Walmart, Giant Landover, Grocery Outlet, Jewel, Kroger, Schnucks, Target, C&S, Bozzuto’s, Brookshire Grocery, Meijer, Food City, KeHe, Lipari, Publix, Merchants Dis Hickory, PDI/Hy-Vee, River Valley, SpartanNash, Supervalu, and UNFI. The sell by date is printed in black inside the cheese bread image on the front on the pizza.Consumers who purchased one of the recalled lots listed above may contact Champion Foods LLC directly [email protected] for more information. For media inquiries, please contact [email protected] recall is being conducted in coordination with FDA.

Foster Poultry Farms, LLC, a Livingston, Calif. establishment, is recalling approximately 3,843,040 pounds of chicken corn dog products that may be contaminated with extraneous material, specifically pieces of wood embedded in the batter, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products subject to recall were produced between July 30, 2024, through August 4, 2025. A list of the products subject to recall can be found here: [view product list]. The labels for the impacted products can be found here: [view labels]. The products subject to recall bear establishment number “P-6137B” either inside the USDA mark of inspection or printed on the packaging. These items were shipped to retail and institutional locations nationwide, including Department of Defense and USDA Commodity Foods donations. While the products were distributed to schools, it resulted from commercial sales and not part of food provided by the USDA for the National School Lunch Program. The problem was discovered after FSIS received a consumer complaint involving an injury from consumption of these products. Additionally, the establishment received multiple consumer complaints, 5 of which involved injuries. Anyone concerned about an injury should contact a healthcare provider.  FSIS is concerned that some products may be in consumers’ refrigerators and freezers, along with institution refrigerators and freezers. Consumers and institutions 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 Foster Farms Consumer Affairs at 1-800-338-8051, from 8 a.m. to 5 p.m. Pacific Time, Monday through Friday or email [email protected]. For media inquiries, please contact [email protected]. Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to [email protected]. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Aug. 22, 2025 - Blue Bell Ice Cream has issued a voluntary recall of a limited quantity of its Moo-llennium Crunch Ice Cream. The recall affects half-gallon packages that were mistakenly packaged in Chocolate Chip Cookie Dough cartons but have a Moo-llennium Crunch lid. The product, produced at Blue Bell's Brenham, Texas, plant, contains undeclared almonds, walnuts, and pecans. The company warned that individuals with allergies or severe sensitivities to these nuts could face serious or life-threatening reactions if they consume the affected ice cream. A Blue Bell employee discovered the packaging error while restocking at a retail location. To date, no illnesses or adverse reactions have been reported, and no other packaging errors have been identified. The affected ice cream can be identified by the code 061027524 on the top of the half-gallon lid. It was distributed through retail outlets in Alabama, Arkansas, the Florida Panhandle, Northwest Georgia, Southern Indiana, Southern Illinois, Kansas, Kentucky, Louisiana, Mississippi, Missouri, New Mexico, Oklahoma, Tennessee, Texas, and Southwest Virginia. Consumers who purchased the affected product can return it to the place of purchase for a full refund. For further information, consumers can contact Blue Bell at 979-836-7977, Monday through Friday, 8 a.m. to 5 p.m. CST, or email [email protected].

Kraft Heinz Foods Company – Oscar Mayer Turkey Bacon Due to Possible Listeria Contamination  July 2, 2025 – Kraft Heinz Foods Company, a Newberry, S.C., establishment, is recalling approximately 367,812 pounds of fully cooked turkey bacon products that may be adulterated with Listeria monocytogenes (Lm), the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today. The turkey bacon was produced from April 24, 2025, through June 11, 2025. The following products are subject to recall:   12-oz. vacuum-packed packages of "Oscar Mayer Turkey BACON ORIGINAL" and universal product code (UPC) "071871548601" printed on the packaging under the barcode, "use by" dates ranging "18 JUL 2025" to "02 AUG 2025," and lot code "RS40." 36-oz. packages containing three 12-oz. vacuum-packed packages of "Oscar Mayer Turkey BACON ORIGINAL" and universal product code (UPC) "071871548748" printed on the packaging under the barcode, "use by" dates ranging "23 JUL 2025" to "04 SEP 2025," and lot codes "RS19," "RS40," or "RS42." 48-oz. packages containing four 12-oz. vacuum-packed packages of "Oscar Mayer Turkey BACON ORIGINAL" and UPC "071871548793" printed on the packaging under the barcode and "use by" dates ranging "18 JUL 2025" to "04 SEP 2025," and lot codes "RS19," "RS40," or "RS42." The products subject to recall bear the USDA mark of inspection on the front of the label. These items were shipped to retail locations nationwide and some were exported to the British Virgin Islands and Hong Kong. The problem was discovered after the establishment's laboratory testing indicated the product may be contaminated with Lm. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider. Consumption of food contaminated with Lm can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected. Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food. FSIS is concerned that some products 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 regarding the recall can contact Kraft Heinz Food Company consumer hotline at 1-800-280-7185 or email [email protected]. Media with questions can contact Lynsey Elve, Director of Global Corporate Communications, Kraft Heinz Food Company at [email protected].  Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to [email protected]. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Trinidad Benham Corp – Dried Black Bean Withdrawal   Withdrawal of Black Beans, Dried, net wt. 16 OZ (1 LB) 454g, packaged in plastic bag. UPC 0 70552 70412 1.  Impacted Lot: Best if used by date of October 7, 2025. DISTRIBUTED BY: WinCo Foods, LLC, BOISE, ID 83704, in AZ, CA, ID, and OR.  Withdrawal due to Elevated levels of MBC (carbendazim) thiophanate-methyl.   BEST IF USED BY 07OCT25 W Code interpreted as follows: 07: Day of Month Produced OCT: Month Produced 25: Year produced plus 1 W: Plant designator = Moses Lake, WA   For More information, visit FDA.gov

Frito-Lay today issued a recall of a limited number of 13 oz. bags of Lay’s Classic Potato Chips that may contain undeclared milk, after being alerted through a consumer contact. Those with an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume the recalled product. The product included in this recall was distributed to certain retail stores and e-commerce distributors in Oregon and Washington. Consumers would have been able to purchase these chips as early as November 3, 2024. No allergic reactions related to this matter have been reported to date. No other Lay’s products, flavors, sizes or variety packs are recalled. The recalled product is in a flexible bag, and the specific information is listed below:   Product Description  Size  UPC  Code Date & Manufacturing Code Representative Image  Lay’s Classic Potato Chips 13 oz.(368.5 grams) 28400 31041 Must have both“Guaranteed Fresh” date of11 FEB 2025ANDone of the following theManufacturing Codes6462307xxOR6463307xx See Image Below If consumers have an allergy or 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 above can contact Frito-Lay Consumer Relations at 1-800-352-4477 (9 a.m. – 4:30 p.m. CST, Monday-Friday).  

Dec. 11, 2024 - Riverside Natural Foods Inc. Issues Voluntary Recall of Select MadeGood® Granola Bar Products over Potential Presence of a Piece of Metal Riverside Natural Foods Inc. is voluntarily recalling certain batches of MadeGood® granola bars due to the potential presence of a piece of metal in the product, which, if consumed, may result in a safety hazard. The health and safety of our consumers is our highest priority. This recall is being initiated as a precautionary measure; no injuries have been reported. Specific products impacted by this recall include the following MadeGood® products: Chocolate Chip Granola Bars, Mixed Berry Granola Bars, Strawberry Granola Bars, Cookies & Crème Granola Bars, Chocolate Banana Granola Bars, Chocolate Drizzled Birthday Cake Granola Bars, Chocolate Drizzled Cookie Crumble Granola Bars, and Chocolate Drizzled Vanilla Granola Bars. Recalled products were produced between January and November 2024 and distributed throughout Canada, the United States and other international markets. Product UPCs and best by dates included in the recall can be found here: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/riverside-natural-foods-inc-issues-voluntary-recall-select-madegood-granola-bar-products-over?utm_medium=email&utm_source=govdelivery.  The company is conducting the voluntary recall with the knowledge of regulatory authorities and working closely with retailers for the removal of recalled products from store shelves. Consumers who have purchased these products are asked to check them against the list and return the recalled product to the store where they bought it for a full refund. The health and safety of our consumers is our highest priority. If you have questions regarding the recall, please contact the MadeGood Consumer Hotline at 855-215-5695 between 8am and 5pm EST. For more information, visit the MadeGood website.    

Oct. 11, 2024 - BrucePac Recalls Ready-To-Eat Meat and Poultry Products Due to Possible Listeria Contamination.For the most up-to-date list of affected items, please visit the FSIS BrucePac Recall Announcement.         BrucePac, a Durant, Okla. establishment, is recalling approximately 9,986,245 pounds of ready-to-eat (RTE) meat and poultry 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 meat and poultry items were produced from June 19, 2024, to October 8, 2024. These products were shipped to other establishments and distributors nationwide then distributed to restaurants and institutions. Information regarding product labels and the list of products will be provided when available. The products subject to recall bear establishment numbers "51205 or P-51205" inside or under the USDA mark of inspection. The problem was discovered after FSIS performed routine product testing of finished product containing RTE poultry products produced by BrucePac and confirmed those products positive for Listeria monocytogenes. Subsequent FSIS investigation identified BrucePac RTE chicken as the source of the Listeria monocytogenes. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider. 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 available for use in restaurants, institutions, and other establishments. These other establishments may have used affected meat and poultry in RTE products that may be on store shelves or in consumers’ refrigerators or freezers. Restaurants, institutions, and other establishments are urged not to serve or use 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. Media and consumers with questions regarding the recall can contact Jeff Golangco, VP Business Development at BrucePac, at 503-874-3000. Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to [email protected]. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.   Company Information BrucePac Durant, OK Establishment ID: M51205+P51205+V51205 Processing Category: Fully Cooked - Not Shelf Stable   Company Contact Information Company Contact BrucePac Jeff Golangco, VP Business Development 503-874-3000   FSIS Contact Information Media Contact Congressional and Public Affairs Kenneth King [email protected]         

Odor-Eaters® Issues Voluntary Nationwide Recall of Specific Lots of Odor- Eaters® Spray Powder and Odor-Eaters® Stink Stoppers® Spray Due to Benzene Contamination Odor-Eaters®, owned by Blistex Inc., is voluntarily recalling a total of forty-one lots of two Odor-Eaters® spray products to the consumer level due to the presence of benzene. Internal testing identified low levels of benzene contamination in specific lots of these aerosol products. Risk Statement: Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. To date, Odor-Eaters® has not received any reports of adverse events related to this recall. The affected Odor-Eaters® spray products are used as antifungal and foot odor-reducing agents and are packaged in aerosol cans. See table below for UPC, lot number and expiration dates. Refer to the image below for guidance on where to find the lot code details on the can. Forty-one lots of two Odor-Eaters® spray products (Odor-Eaters® Spray Powder and Odor-Eaters® Stink Stoppers® Spray) are impacted by this voluntary recall, specifically: Click here to view the affected products list. Beginning on November 18, 2021, at 8am (EST), consumers may access www.odoreatersrecall2021.com to request a product refund, as well as for product images, lot information, and additional information. Consumers with questions regarding this recall can contact 1-855-544-4821 with questions Monday to Friday from 8:00am-5pm (EST). Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using these spray products. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.    

Bayer Issues Voluntary Recall of Specific Lotrimin® and Tinactin® Spray Products Due to the Presence of Benzene Bayer is voluntarily recalling all unexpired Lotrimin® AF and Tinactin® spray products with lot numbers beginning with TN, CV or NAA, distributed between September 2018 to September 2021, due to the presence of benzene in some samples of the products. Benzene is not an ingredient in any of Bayer Consumer Health products. The affected Lotrimin® and Tinactin® spray products are over the counter antifungal products, sold individually or in combo packs. The impacted products are: ·Lotrimin® Anti-Fungal (AF) Athlete's Foot Powder Spray ·Lotrimin® Anti-Fungal Jock Itch (AFJI) Athlete's Foot Powder Spray ·Lotrimin® Anti-Fungal (AF) Athlete’s Foot Deodorant Powder Spray ·Lotrimin® AF Athlete's Foot Liquid Spray ·Lotrimin® AF Athlete’s Foot Daily Prevention Deodorant Powder Spray ·Tinactin® Jock Itch (JI) Powder Spray ·Tinactin® Athlete’s Foot Deodorant Powder Spray ·Tinactin® Athlete’s Foot Powder Spray ·Tinactin® Athlete’s Foot Liquid Spray Product images and information on which lot numbers fall under this recall are available at: https://livewell.bayer.com/document/2011 There are no issues of concern with Lotrimin®/Tinactin® creams, including Lotrimin® Ultra, or any other Bayer products. The recalled products are all packaged in aerosol spray cans. The products were distributed in the U.S., Puerto Rico, Canada and Mexico through a variety of retail channels. . Consumers may request a refund by visiting www.lotrimin.comExternal Link Disclaimer or www.tinactin.com, and may contact Bayer with questions by calling 1-866-360-3266, Monday-Friday between the hours of 8 a.m. and 8 p.m. Eastern Time. A photo of the product will be required to receive a refund. After taking your photo and completing the refund process, please discard the product appropriately. Consumers who have the products that are being recalled should stop using. Consumers should contact their physician or healthcare provider if they have any questions, concerns or have experienced any problems related to using these aerosol antifungal products.