Guidant Corp. voluntarily recalled nearly 50,000 of its cardiac defibrillators worldwide because of potential malfunctions in the devices.

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Guidant Corporation recalled its popular Guidant Intelis II Pacemaker on July 17 th, 2005 because of a manufacturing defect. There have been 69 reports of failure in 18,000 units built between November 1997 and October 2000 because of failure in a seal to keep moisture out of the unit. Once moisture invades the unit it can disrupt the delicate electronics inside causing such damage as:

• Advanced battery depletion
• False reset warnings
• Irregular pacing
• Unnecessary replacement warnings

If you or someone you love has a Guidant Intelis II Pacemaker manufactured between November 1997 and October 2000 with model numbers 1483, 1484, 1485, 1384, 1385, 1349, or 1499, contact your doctor immediately. These devices may need to be replaced, so consult your doctor about the appropriate course of action.

The Law Firms of Steigerwalt & Associates and Provost * Umphrey have joined forces to help victims of serious injury and death as a result of defective and recalled Guidant defibrillators and pacemakers throughout the country. Our firms have spent many years successfully helping injured people and their families with mass tort and defective product cases around the U.S. We are dedicated to pursuing justice for our clients and fighting for the rights of the injured. Together our law firms can help you - regardless of where you live.