St. Jude Medical has issued a warning regarding its implanted defibrillators after reports that a malfunction was linked to two patient deaths. The company said they could stop working after rapidly ...

The U.S. Food and Drug Administration on Wednesday sent a warning letter to Abbott, charging the Chicago-based medical device provider with failing to reveal a deadly defect with defibrillators ...

St. Jude Medical, a medical device company based in St. Paul, Minn., has agreed to pay $3.65 million to resolve allegations that it inflated the cost of pacemakers and defibrillators purchased by the ...

CINNCINNATI, OH — A newly published case report describes a single incident where the Durata (St Jude Medical, St Paul, MN) lead failed at the time of high-voltage shock delivery in a patient with an ...

The Food and Drug Administration has approved St. Jude Medical's new Ellipse implantable cardioverter defibrillator (ICD) and its Assura cardiac resynchronization therapy defibrillator (CRT-D), ...