Device Recalls
More Information on Device Recalls
- Public Citizen to Congress: FDA’s Device Tracking Regulations Weaker than First Proposed, October 29, 2014
- Statement: FDA’s Unique Device Identifier Rule Years Delayed but a Welcome Step Forward for Medical Device Safety, September 20, 2013
- Letter About Defective Welch Allyn AEDs, March 13, 2009
- Letter Condemning Delayed Recall of Defective Intravenous Infusion Pumps, March 12, 2009
- Statement: FDA Negligent in Delayed Response to Problems with Pediatric Breathing Device, March 10, 2009
- Letter Urging an Investigation of Medtronic Defibrillator Recall, October 16, 2007