Guidant Contak Renewal 3 and 4, Renewal 3 and 4 AVT, Renewal RF
guidant recall
Guidant Devices
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guidant contak renewal Information on the Warning from Guidant

Guidant Corp. initially warned physicians about problems with these devices on June 24, 2005.
Problem
A magnetic switch in these devices may stick in the closed position, resulting in a failure of the device to deliver therapy.
Reports of Injuries
As of June 24, 2005, Guidant Corp. announced they had received 4 confirmed reports of this problem occurring with implanted devices. An additional instance is suspect.
Models

The problem affects a number of the models in the line.

H170 H173 H175 H177 H179 H190
H195 H199 M150 M155 M157 M159
M170 M175 M177 M179 H230 H239
Recommendation
Patients should consult with their physicians to discuss treatment options
Documents

Advisory Update to June 23 Letter
Guidant Corp.
August 12, 2005

Letter to Patients
Guidant Corp.
July 15, 2005

Urgent Medical Device Safety Information & Corrective Action
Guidant Corp.
June 24, 2005

Our Lawyers Can Help You

O'Steen & Harrison, PLC presently is handling legal claims on behalf of those injured by defective Guidant heart devices.

For free answers to your legal questions about the Guidant Contak Renewal 3 and 4, Renewal 3 and 4 AVT, or Renewal RF, just call us toll-free at 1-800-883-8888 or submit this online contact form.