Of the 95 acne products the FDA tested, over 90% had undetectable or low levels of benzene. TAMPA, Fla. - The FDA issued a ...

The recalls announced this week apply to stores selling the items. FDA officials said consumers don’t need to take any specific action. The FDA identified the six products after testing 95 acne ...

The FDA later issued its classification of the recall on April 9 ... more than 41,000 bottles across two Proactiv-branded acne treatment products: Proactiv Emergency Blemish Relief and Proactiv ...

The Food and Drug Administration published a notice from Amneal Pharmaceutical that said the company is recalling two lots of ...

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 ...

A Class II recall is the second riskiest of the FDA’s recall classifications and indicates that consumption of the recalled product “may cause temporary or medically reversible adverse health ...