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Friday, June 17, 2005 voluntarily recalled nearly 50,000 of its cardiac defibrillators and pacemakers worldwide because of potential malfunctions in the devices.
Also on July 19, 2005, The NY Times reported that Guidant Corp. “alerted doctors that nine of its older pacemaker models were prone to failure.”
If you or someone you know has had certain Guidant Defibrillator or Guidant Pacemaker implanted or replaced they may be at risk. If so, you or that someone may be entitled to monetary damages.
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