On Wednesday, December 14, 2005, the FDA announced that it has received reports of recent patient deaths linked to fatal complications in heart devices manufactured by Guidant Corporation. Time is limited. Contact Our Lawyers. or Click here to begin your FREE Case Review.

VENTAK PRIZM AVT

The Ventak Prizm AVT provides atrial therapy for people who suffer from potentially fatal heart problems. Guidant has ordered a recall of 21,000 devices due to a flaw in the memory system that may prevent the defibrillator from delivering the appropriate amount of therapy as needed. The Ventak Prizm AVT has twice suffered failures, although there have been no serious injuries or fatalities associated with this failure. Patients who have this device are advised to report as soon as possible to their doctors to receive a necessary programming change.

Ventak Prizm 2 DR | Contak Renewal | Ventak Prizm AVT | Vitality AVT | Renewal 3 AVT | Renewal 4 AVT

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