Posted by Robert H Hilley IV on 11/03/05

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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
recall includes:

Ventak Prizm 2 DR (model 1861)
Contak Renewal (model H135) and Contak Renewal 2 (model
H155)
Ventak Prizm AVT
Vitality AVT
Renewal AVT
Contak Renewal 3 and 4, Renewal 3 and 4 AVT and Renewal RF

Read more about defective defibrillators at:
http://www.schmidtandclark.com

Guidant and Medtronic Defective Defibrillators

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