Search Results

FDA Recalls Enteric-Coated Aspirin Tablets Due To Packaging Mistakes July 2, 2013 The U.S. Food and Drug Administration (FDA) recently announced it would partner with Advance Pharmaceutical, Inc., in implementing the voluntary recall of the company’s enteric-coated aspirin tablets. The recall is being initiated due to a packaging mix up that placed 500 mg acetaminophen tablets in bottles marked as enteric-coated aspirin. Both medications (more...)

FDA Issues Recall On Lots Of Hydrocodone and Acetaminophen January 8, 2012 The U.S. Food and Drug Administration and Mylan, Inc. recently issued a voluntary product recall on several lots of their medications, Hydrocodone and Acetaminophen in 10 and 500-milligram dosages respectively. According to an FDA press release, the recall was issued after certain lots of the medications were found to exceed weight limits and (more...)