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The Guidant internal cardiac defibrillator (ICD) recall includes 50,000 devices that are currently in use, at least 20,000 of which are implanted into American patients. The following is a list of potential risks associated with the recalled ICDs manufactured by Guidant.
Serious complications from the surgery:
Less serious complications:
Guidant Corporation has advised patients to take the following steps in regards to the recent recalls and warnings.
If you are concerned about your Guidant ICD, contact the law firm of Miller & Associates. Their experienced product liability lawyers will guide you through your options during a free and confidential consultation. Contact their law firm today.
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A statement released yesterday by the U.S. Food and Drug Administration urged patients with potentially defective models of Boston Scientific/Guidant pacemakers and defibrillators to schedule an exam with their physicians as soon as possible.
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Guidant defibrillators have been implanted into thousands of cardiac patients and are used t...
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