Ancure is the registered name for a "stent-graft" device used to treat abdominal aortic aneurysm without traditional surgical techniques. The medical device, part of the Ancure Endograft System, uses a catheter to insert a sheath through the femoral artery in the leg. The device was marketed as allowing physicians to repair bulges in the aorta without performing a major open surgery that can result in significant complications.

The Ancure device was made by Endovascular. On June 12, 2003, federal prosecutors charged Endovascular Technologies with 10 felony counts, including false statements to the Food and Drug Administration (FDA) in connection with the Ancure device.

"At least 75 patients died and 991 were injured after receiving Ancure implants," according to Food and Drug Administration records. Lawsuits charge that at least some were the result of the implants.

If you or your loved one has been the recipient of a defective Guidant Ancure device, please submit the accompanying form. You may be entitled to monetary awards for your injury!