Post: Defective Defibrillators
Posted by Robert H Hilley IV on 11/03/05
On June 17, 2005, Guidant recalled more than 50,000 of its
defective cardiac defibrillators implanted in patients
because of potential malfunctions in the devices. The
Ventak Prizm 2 DR (model 1861)
Contak Renewal (model H135) and Contak Renewal 2 (model
Ventak Prizm AVT
Contak Renewal 3 and 4, Renewal 3 and 4 AVT and Renewal RF
Read more about defective defibrillators at:
Guidant and Medtronic Defective Defibrillators
Posts on this thread, including this one
- Defective Defibrillators, 11/03/05, by Robert H Hilley IV.
- Re: Defective Defibrillators, 11/03/05, by Tom Collen.