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Health · 7h

FDA Announces Recall of Repackaged M&M's Due to Dangerous Allergy Risk

The products, repackaged by Beacon Promotions Inc., may contain undeclared milk, soy, and peanut allergens.

Blavity on MSN · 1h

M&M recall: FDA issues high risk warning on thousands of repackaged candies in 20 states

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FDA recalls mislabeled M&M’s sold in Texas over missing allergen warnings

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If you recently bought M&M’s in these 20 states, the FDA says you need to check this now

More than 6,000 units of M&M’s candies distributed to 20 states, including Alabama, have been recalled, according to the U.S. Food and Drug Administration.

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FDA Announces Recall of Repackaged M&M’s Candies in 20 States

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Check your kitchens: These M&Ms sold in 20 states might contain serious allergens

Dagens.com on MSN

FDA recalls cholesterol medication nationwide

The recall involves tens of thousands of bottles distributed nationwide.

Hoodline

FDA Issues Nationwide Recall of 20,000 Bottles of Triglyceride Medication Due to Oxidation Concerns

The FDA announced a recall of over 20,000 bottles of a triglyceride medication due to an oxidation issue that may lead to leakage and inconsistent treatment.

FDA announces FreeStyle Libre continuous glucose monitor sensor recall

Abbott Diabetes Care has recalled some of its FreeStyle Libre 3 and FreeStyle Libre 3 Plus glucose monitor sensors for people with diabetes.

1don MSN

Cake mix recall upgraded to highest FDA risk level due to undeclared allergen

Hundreds of bags of cake mix pulled last year were bumped up to the U.S. Food and Drug Administration’s most high-risk recall category. In December, B.C. Williams Bakery Service — a Dallas-based distribution company that specializes in wholesale baking ingredients — issued a recall for three varieties of its 50-pound cake mix bags.

6abc Action News

FDA recall: Erectile dysfunction drug found in honey energy supplement

The FDA issued a recall Wednesday for a honey energy supplement after an undeclared erectile dysfunction medication was found in the product.

WBIW

FDA raises alarm: 80,000+ McCafé Decaf K-Cups recalled over caffeine risk

INDIANA— Coffee drinkers in three states are being warned to double-check their morning brew. The U.S. Food and Drug Administration (FDA) has officially designated