Walmart Issues Recall
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The FDA classifies this recall as Class II, which the agency describes as a situation "in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote."
Alembic, Sun and Glenmark issue US drug recalls due to the presence of carcinogens or foreign matter
A trio of Indian drugmakers—Alembic Pharmaceuticals, Sun Pharmaceutical and Glenmark Pharmaceuticals—issued separate voluntary U.S. drug recalls in recent weeks due to either the presence of carcinogens or foreign matter in the products.
Fromi, a cheese maker that sells out of New York, is working with the U.S. Food and Drug Administration (FDA) to recall 12 cases of its Brie Royal Faucon cheese because they may be contaminated with Listeria monocytogenes, a bacterium that can cause potentially serious infection in vulnerable populations.
From August 19, 2025, the FDA announced that B. Braun Medical Inc. (B. Braun) is voluntarily recalling 2 lots of its Lactated Ringer’s Injection, USP, 1000 mL and 0.9% Sodium Chloride Injection, USP, 1000 mL to hospitals because of the presence of particulate matter in the containers.
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PRIMETIMER on MSNWhat’s behind the FDA Recall of nearly 2,000 cases of 7Up Zero Sugar?
Mislabeling sparks recall of 7Up Zero Sugar, raising concerns for those monitoring sugar intake.
The U.S. Food and Drug Administration has elevated the recall of a dessert dip previously sold at Aldi to Class II, meaning that the "product may cause temporary or medically reversible adverse health consequences," per the FDA website.
Some imported cookware made with certain materials may leach "significant levels" of lead into food, which can cause serious health effects, the FDA said.
Dollar General Corporation is recalling three lots of its Clover Valley Instant Coffee due to potential glass contamination. The recall affects 8-ounce packages of Clover Valley Instant Coffee with UPC 876941004069, specifically lots L-5163, L-5164, and L-5165, with best by dates in December 2026, the Food and Drug Administration said.