Medical Device Manufacturer Guidant Charged in Failure to Report Defibrillator Safety Problems to FDA
Medical Device Manufacturer Guidant Charged in Failure
to Report Defibrillator Safety Problems to FDA
Medical device manufacturer Guidant LLC, a wholly-owned subsidiary of Boston Scientific Corporation, was charged today with criminal violations of the Federal Food, Drug, and Cosmetic Act related to safety problems with some of its implantable defibrillators.
Go to Source