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    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
    recall includes:

    Ventak Prizm 2 DR (model 1861)
    Contak Renewal (model H135) and Contak Renewal 2 (model
    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:

    Guidant and Medtronic Defective Defibrillators

    Posts on this thread, including this one

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