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proven results

$240 Million Guidant Defibrillator Settlement

KCR clients who were injured by malfunctioning Guidant cardiac defibrillators will claim shares of the $240 million fund as part of a 2008 nationwide settlement.

Guidant Recall News

Boston Scientific / Guidant Recall: Questions & Answers
FDA Web site — August 10, 2007

FDA Update Statement on Boston Scientific/Guidant Pacemakers and Defibrillators
FDA Web site — July 11, 2006

FDA study reveals malfunctions in implanted heart defibrillators were on the rise well before Guidant recall
MSNBC News — Sept. 16, 2005

FDA Updates Consumers on Guidant Corporation’s Implantable Defibrillators
FDA Web site — July 2005

FDA Announces Guidant’s Class I Pacemaker Recall
FDA Web site — July 2005

FDA Issues Nationwide Notification of Recall of Certain Guidant Implantable Defibrillators and Cardiac Resynchronization Therapy Defibrillators
FDA Web site — June 2005

 

 

 

Boston Scientific/Guidant Pacemakers and Guidant Cardiac Defibrillators Recalls

Boston Scientific/Guidant Pacemakers and Guidant Cardiac Defibrillators Recalls

 

Guidant Pacemakers Recall

defective guidant pacemakersIn July 2005, thousands of Guidant pacemakers were recalled because of a defective “sealing component” that allowed fluid to leak into the device. The recall notice warns patients and doctors that the faulty pacemakers may need to be replaced, requiring another surgery.

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Guidant Cardiac Defibrillators Recall

guidant cardiac defibrillator recallIn June 2005, Guidant recalled nearly 80,000 of its cardiac defibrillators because of defects that could lead to serious injury and death. Reports indicate that approximately 38,000 of the recalled defibrillators were implanted in patients throughout the United States.

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If you or someone you know has an implanted Guidant pacemaker or Guidant cardiac defibrillator matching one of the recalled models, fill out and submit the contact form on this page for a free case evaluation or call us toll-free at (888) 285-3333.

 

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