 |
RENEWAL 3 AVT Recall
RENEWAL 3 AVT is a device designed to provide atrial therapy. These products are subject to the
Guidant recall and suffer from a memory error which may eliminate the availability of certain therapies. Two incidents of failure
have been noted for devices that provide atrial therapies, including the RENEWAL 3 AVT. Neither of these failures was
reported to cause a patient death or serious injury. These failures were reported from a group of 21,000 devices implanted worldwide,
including 18,000 that have been implanted in the United Sates. Guidant has recommended a programming change that can reduce
the risk of injury or death due to this product defect.
Back to list of Guidant defective products.
About the Sponsors of this Pacemaker and Defibrillator Information Website
If you or a loved one has been injured due to a defective pacemaker or defibrillator product manufactured by Guidant, you
may be entitled to compensation. The sponsors of this website are attorneys who specialize in helping those who have been injured
by defective products. Please contact our offices today so that one of our Guidant lawyers may answer any questions that you
have and provide a free case review if needed. Our toll-free number is 888-255-AWKO (2956).
If warranted, we can file a Guidant lawsuit to help obtain the proper compensation.
The sponsors of this website include: Aylstock, Witkin & Sasser, Guidant Litigation Group; Neblett, Beard & Arsenault;
Andrus, Boudreaux, Lemoine & Tonore; Lundy & Davis, LLP; and Barrios, Kingsdorf & Casteix, LLP.
|
|
|
|
