Device malfunction in Guidant Implantable Cardiac Defibrillators has potentially fatal consequences
Implantable Cardiac Defibrillators (ICD) marketed by Guidant Corp. have been recalled because of a device malfunction that can lead to potentially fatal consequences. On June 17, 2005, in the first of multiple recalls, the FDA issued a nationwide notification of recall of certain Guident implantable defibrillators because of short circuiting issues that could lead to a failure of the device to deliver a life-saving shock when it was supposed to.
A later recall issued on April 5, 2007 recalled defective defibrillators and pacemakers marketed by Boston Scientific/Guidant claiming the devices were subject to rapid battery depletion and premature device failure.
Because defibrillators and pacemakers are used to preserve the lives of persons who depend on them, the failure of these devices can lead to very serious injuries and death.
More information on the defective Guidant Defibrilltor recalls can be found on our Medical Injury Lawyer website.
