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

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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

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

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

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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

Source: FDA Food Safety Recalls RSS Feed

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

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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 w

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

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

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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

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

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

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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

Source: FDA Food Safety Recalls RSS Feed

Golden State Medical Supply, Inc. Issues a Voluntary Nationwide Recall of Atenolol 25 mg Tablets and Clopidogrel 75 mg Tablets Due to a Label Mix-up

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Golden State Medical Supply, Incorporated (GSMS, Inc.) - Camarillo, CA has initiated a voluntary recall of the products listed in the table below because a report was received that a bottle containing Clopidogrel 75mg Tablets produced with lot# GS046745 was mislabeled as Atenolol 25mg Tablets. This

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

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

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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 react

Source: FDA Food Safety Recalls RSS Feed

Momyer Distribution Inc. Issues Allergy Alert on Undeclared Milk in Dark Chocolate Almonds

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Momyer Distribution Inc of Salem, Oregon is recalling Dark Chocolate Almonds because they may contain undeclared milk.

Source: FDA Food Safety Recalls RSS Feed

Eugia US LLC Issues Voluntary Nationwide Recall of Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), Due to the Presence of Particulate Matter

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East Windsor, New Jersey, Eugia US LLC (formerly AuroMedics Pharma LLC) has initiated a voluntary recall of lot number AC22006 of AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), 10 mL single dose vial to the consumer level from the U.S. market due to a product complaint for the pr

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

Eugia US LLC Issues Voluntary Nationwide Recall of Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), Due to the Presence of Particulate Matter

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East Windsor, New Jersey, Eugia US LLC (formerly AuroMedics Pharma LLC) has initiated a voluntary recall of lot number AC22006 of AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), 10 mL single dose vial to the consumer level from the U.S. market due to a product complaint for the pr

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