Cranial Drill Recall: Integra LifeSciences Recalls Codman Disposable Perforators Due to Risk of Device Disassembly

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program

The Food and Drug Administration is advising consumers not to purchase or use Power Plus Desire, a product promoted and sold for sexual enhancement on various websites and possibly in some retail stores.

Commerce, CA – Koikoi Trading Inc. is recalling certain lots of FU ZHOU FISH BALL products in multiple pack sizes (200g, 400g, and 5LB) because the products may contain undeclared allergens: wheat and sesame. People who have an allergy or severe sensitivity to wheat and/or sesame run the risk of a s

FDA-TRACK: Prescription Drug User Fee Act Procedural Goals Summary

ANDAs: Pre-Submission Facility Correspondence Related to Prioritized Generic Drug Submissions

Meeting Presentations. CDER professionals participate in several meetings, conferences and workshops throughout the year. Appealing primarily to the pharmaceutical industry and health care professionals, topics can range from users fees, to drug advertising and marketing, to genomics, to over-the-co