If you’re one of the 50 million Americans dealing with acne, the FDA has a warning about a recent skincare recall that might ...

The recall, which is still ongoing, affects more than 41,000 bottles across two Proactiv-branded acne treatment products.

The risk level of the recall has been classified as a 'Class II', meaning 'it may cause temporary or medically reversible ...

When you learn about a recall involving an FDA-regulated product that you or a loved one has purchased or used, there are several pieces of information you need in order to make informed decisions ...

per the FDA. The salad dressing was produced at a regional facility and distributed to limited Trader Joe’s locations in Ohio and other states. No customer complaints have been reported to date.

Frozen meals, snacks, cat food, and cheesecake are just a few items listed in March on the Federal Food and Drug Administration website. It can feel like a job just keeping up with what the FDA ...

US FDA recalled a brand of coffee grinds from 15 states as they were mislabeled as decaffeinated and may lead to “adverse health consequences.” US Food and Drug Administration (FDA) recalled a ...

The FDA recalled over 4,000 bags of ground coffee mislabeled as decaffeinated across 15 states. The recall applies to 12-ounce bags of Our Family's Traverse City Cherry Decaf Light Roast.

The recall was voluntarily issued on March 13 by Massimo Zanetti Beverage USA, one of the largest suppliers of coffee in the U.S. The FDA classified the recall with a "category II" label ...