The Food and Drug Administration Feb. 5 released an alert notifying patients of a safety concern using diabetes devices such ...
More than 2 million cases of baked goods distributed throughout the nation are being recalled this year due to the possible ...
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Hosted on MSNMore Than 2 Million Cases of Popular Donuts & Pastries Recalled in the U.S. & CanadaApproaching Valentine's Day, the FDA has a warning on 60 varieties of sweets "within expiration"...including from a beloved ...
The U.S. Food and Drug Administration (FDA) has given its second most serious risk level, Class II, to a product from D. Coluccio & Sons. The recalled product is a 300 gram pack of chocolate chip ...
For individuals who do not belong to vulnerable groups, listeria infection—otherwise known as listeriosis—usually causes food poisoning symptoms such as fever, muscle aches, fatigue, headaches, ...
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The Healthy on MSNNearly 7,000 Bottles of a Heart and Diabetes Medication Recalled in At Least One StateAround 20 million Americans reportedly trust this medication—here are the recall details, and the unusual error that caused it.
Although it didn’t initially have a classification, it was given a Class II recall on January 21. According to the FDA, that classification is a “situation in which use of or exposure to a ...
Owners may contact Ford customer service at 1-866-436-7332. Ford's number for this recall is 25S02. Vehicles in this recall were previously repaired under 24V-267 and will need to have the new ...
Although it didn’t initially have a classification, it was given a Class II recall on January 21. According to the FDA, that classification is a “situation in which use of or exposure to a violative ...
First Aid Beauty has issued a voluntary recall of its popular Ultra Repair Cream in Coconut Vanilla scent after more than 2,500 jars that were meant to be quarantined were mistakenly distributed.
The FDA issued a recall for the second-highest recall classification out of three tiers. Here's what we know about why the skin care product was recalled and why. The FDA issued a Class II recall ...
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