Law Firms file Class Action after Guidant Recalls Defibrillators

June 20, 2005 - Manhattan law firms have jointly filed a class action lawsuit on behalf of patients implanted with malfunctioning defibrillators manufactured by Guidant Corporation. Read More

FDA Recalls Guidant Defibrillators

June 17, 2005 - FDA is notifying health care providers and patients that the Guidant Corporation is recalling certain of its implantable defibrillators and cardiac resynchronization therapy defibrillators. Read More

FDA Public Health Notification: Problems with Endovascular Grafts

April 27, 2001 - This letter is to inform you about serious problems that have occurred with two endovascular prosthetic graft devices used to treat infrarenal AAA, and to make recommendations concerning... Read More

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