Kraft Heinz Issues Voluntary Recall of Select Kraft Singles American Processed Cheese Slices

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Kraft Heinz is announcing a voluntary recall of approximately 83,800 cases of individually-wrapped Kraft Singles American processed cheese slices that were shipped to a limited number of customers. The voluntary recall comes as a precaution after a temporary issue developed on one of our wrapping ma

Source: FDA Food Safety Recalls RSS Feed

Life Raft Treats has Expanded their Recalls of Ice Cream Products, Not Fried Chicken And Life Is Peachy, Due to Possible Listeria Monocytogenes Contamination

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Life Raft Treats is expanding their recall of their Not Fried Chicken 64 oz bucket, Not Fried Chicken 2.5 oz bar UPC 8 60006 18210 6 and Life Is Peachy 6 count box ice cream products, to include the BEST BY DATES up
to and including AUG 08282024 due to a potential contamination of Listeria monocytog

Source: FDA Food Safety Recalls RSS Feed

Knickerbocker 365 Issues Allergy Alert on Undeclared Milk in “Homestyle Hamburger Buns”

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Knickerbocker 365, Inc. of Madison Heights, MI, is recalling its 16-ounce packages of "Homestyle Hamburger Buns" because they contain undeclared milk.

Source: Food and Drugs Administration--Recalls/Safety Alerts

Church & Dwight Issues Voluntary Nationwide Recall of One Specific Lot of TheraBreath Strawberry Splash for Kids 16oz Sold Exclusively on Amazon Between May 31 and September 02, 2023, Due to Microbial Contamination Identified as Yeast (Candida Parapsilosis)

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FOR IMMEDIATE RELEASE – September 13, 2023 – EWING, N.J – Church & Dwight Co., Inc. (NYSE:CHD) today initiated a voluntary recall of one specific lot of TheraBreath Strawberry Splash for Kids 16oz after the Company identified a microbial contamination due to the presence of yeast (Candida Parapsilo

Source: Food and Drugs Administration--Recalls/Safety Alerts

Universal Meditech Inc. Expands Nationwide Recall to All Products Manufactured between March 2021 and November 2022

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Universal Meditech Inc. initiated a nationwide recall of products it manufactured between March 2021 and November 2022. The recall is due to the reasons that: i. The company is going out of business, hence would not be able to continue fulfilling any post-market responsibilities of these distributed

Source: Food and Drugs Administration--Recalls/Safety Alerts

Sheng Kee of California, Inc. Issues Allergy Alert on Undeclared Egg in the Following Traditional Mooncake Products

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Sheng Kee of California, Inc. is voluntarily recalling varieties of Mooncake Gift Boxes for customers that have any issues because they may contain undeclared egg wash. People who have allergies to egg run the risk of serious or life-threatening allergic reaction if they consume these products.

Source: Food and Drugs Administration--Recalls/Safety Alerts

Novartis Issues Voluntary Nationwide Recall of One Lot of Sandimmune® Oral Solution (Cyclosporine Oral Solution, USP), 100 mg/mL Due to Crystallization

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Novartis is conducting a voluntary nationwide recall at the consumer level of one lot of its Sandimmune® Oral Solution (cyclosporine oral solution, USP), 100 mg/mL in the US due to crystal formation observed in some bottles, which could potentially result in incorrect dosing. No other Sandimmune for

Source: Food and Drugs Administration--Recalls/Safety Alerts

Church & Dwight Initiates Voluntary Recall of One Specific Lot of TheraBreath Kids Strawberry Splash 16oz Sold Exclusively on Amazon Between May 31 and September 02, 2023, Due to an Isolated Manufacturing Issue

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FOR IMMEDIATE RELEASE – September 8, 2023 – EWING, N.J – Church & Dwight Co., Inc. (NYSE:CHD) today initiated a voluntary recall of one specific lot of TheraBreath Kids Strawberry Splash 16oz after the
Company identified a microbial contamination due to the presence of yeast (Candida Parapsilosis)

Source: Food and Drugs Administration--Recalls/Safety Alerts

OBC Group Corp Retira Del Mercado Productos De Semillas Y Cápsulas De Nuez De La India Debido A Posibles Riesgos Para La Salud

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OBC GROUP CORP de, Miami, FL está retirando del mercado sus semillas y capsulas NUT DIET MAX Nuez de la India porque un análisis de la FDA ha determinado que los productos parecen ser Thevetia peruviana o adelfa amarilla. Se sabe que todas las partes de la planta de adelfa amarilla contienen glucósi

Source: Food and Drugs Administration--Recalls/Safety Alerts

OBC Group Corp Recalls Nuez de la India Seeds and Capsules Products Due to Possible Health Risks

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OBC GROUP CORP of, Miami, FL is recalling its NUT DIET MAX Nuez de la India Seeds and Capsules because FDA analysis has determined that the products appear to be Thevetia peruviana, or yellow oleander. All parts of the yellow oleander plant are known to contain cardiac glycosides that are highly tox

Source: Food and Drugs Administration--Recalls/Safety Alerts