FDA recalls over 4,000 bags of ground coffee mislabeled
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Frozen meals, snacks, cat food, and cheesecake are just a few items listed in March on the Federal Food and Drug Administration website.
A Class I recall is issued by the U.S. Food and Drug Administration in situations that can have deadly consequences.
The Food and Drug Administration has identified a Class I recall of Medtronic Aortic Root Cannulas due to a risk of unexpected loose material in the male luer used in the cannula.
The U.S. Food and Drug Administration has issued its highest-risk warning for a hot pot sauce recalled earlier this month. The sauce, which was imported from China and sold in California, has been recalled due to undeclared allergens that could pose life-threatening risks.
Coffee lovers will need to double-check the label of their favorite morning pick-me-up beverage.
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Woman's World on MSNFDA Recalls Coffee After Labeling Mix-Up—It Wasn’t Really Decaf!More than 60 percent of Americans begin their mornings with a cup of coffee. While many reach for it for a caffeine boost, others simply enjoy the ritual and flavor, choosing decaf instead. Recently,
All Coca-Cola lovers in Illinois should be aware of a recent recall by the U.S. Food and Drug Administration. The FDA issued a voluntary recall of 864 12-packs of Coca-Cola being sold in Illinois and Wisconsin earlier this month, classifying it as a Class II recall on March 24.
A batch of Our Family Traverse City Cherry decaf coffee may not be caffeine-free due to a labeling mistake. The FDA has issued a recall across 15 states, warning that the mix-up could be risky for certain consumers.
Coca-Cola has issued a recall of select soda packs due to foreign object contamination. The drink brand initially recalled specific 12-packs of Coca-Cola 12-oz. cans on March 6. On Monday, March 24, the U.S. Food and Drug Administration (FDA) classified it as a Class II recall, meaning that the risk is remote.