UBI Pharma Inc. – 10/14/2025

FDA is making optimal use of its financial resources to maximize its ability to efficiently and effectively deliver on its commitments to the public.

Medline is recalling certain Medline Kits containing recalled Medtronic DLP Left Heart Vent Catheters as the catheter may not retain its shape.

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

A user fee program for nonprescription (over-the-counter or OTC) monograph drugs would be a potential funding mechanism to supplement congressional non user-fee appropriations.

CENTER VALLEY, Pa., (January 16, 2026) — Olympus Corporation has announced the expansion of a previous global medical device removal action for ViziShot 2 FLEX (19G) EBUS -TBNA needles (“ViziShot 2 FLEX”) after receiving and investigating complaints of device components ejecting or detaching during

Failure to Register and List