Medical Device Reporting for People Injured by Vaginal Mesh, Actos, Fosamax, and DePuy ASRs: What the Consumer Needs to Know

Manufacturers, user facilities and importers of medical devices are mandated to submit certain adverse events to the U.S. Food and Drug Administration [FDA].  Medical device reporting requires that manufacturers report to the FDA when they learn that one of their devices may have contributed to a death or serious injury.  Consumers and health professionals can [...]