Arterial Cannula Recall: Edwards Lifesciences Removes Arterial Cannula due to Risk of Wire Exposure

Sandoz, Inc. (“Sandoz”) is initiating a voluntary recall of one (1) lot of Cefazolin for Injection, USP, 1 gram per vial.

July 18, 2025: Meeting of the Psychopharmacologic Drugs Advisory Committee Meeting Announcement

FDA has determined that a REMS is no longer necessary to ensure ERA medicines’ benefits outweigh the risk of EFT.

CGMP/Finished Pharmaceuticals/Adulterated

The Food and Drug Administration is advising consumers not to purchase or use ZapMax, a product promoted and sold for sexual enhancement on various websites, including www.amazon.com, and possibly in some retail stores.

Unlawful Sale of Unapproved and Misbranded Drugs to United States Consumers Over the Internet