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. Call us Toll Free at 1-866-722-8700 or Click here to begin your FREE Case Review.

RENEWAL 3 AVT   

Guidant is ordering a recall of their popular Renewal 3 AVT atrial therapy device due to a memory error which may prevent the device from recognizing a critical situation. There have been approximately two failures in the 21,000 devices in use around the world, but neither of these failures have resulted in serious injury or death. People who have this device are recommended to report to their doctor immediately for an important programming change that will hopefully compensate for the initial failure.

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

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