$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.
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

In
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.
In
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.
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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