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Guidant Defibrillators

WHILE QUESTIONS LINGER OVER GUIDANT’S THREE-YEAR DELAY IN NOTIFYING DOCTORS OF THE RISK ITS IMPLANTED DEFIBRILLATORS COULD SHORT-CIRCUIT, CARDIOLOGISTS

Jun 19, 2005 | www.Newsinferno.com
In hindsight, there is no doubt that, while Guidant Corporation maintained its internal heart defibrillator (the Ventak Prizm 2 DR) was safe and...

FDA Issues Nationwide Notification of Recall of Certain Guidant Implantable Defibrillators and Cardiac Resynchronization Therapy Defibrillators

Jun 17, 2005 | www.fda.gov
FDA is notifying health care providers and patients that the Guidant Corporation is recalling certain of its implantable defibrillators and cardiac...

FOLLOW-UP: GUIDANT CONTINUED TO SELL HEART DEFIBRILLATOR FOR IMPLANTATION IN PATIENTS EVEN AFTER BECOMING AWARE OF A DEFECT WHICH COULD CAUSE THE DEVICE TO SHORT-CIRCUIT AND FAIL

Jun 3, 2005 | www.Newsinferno.com
Despite the fact that company officials were aware of an electrical defect which had caused some of its internal heart defibrillators to...

Guidant Sold Faulty Defibrillators After New Ones Were Available

Jun 3, 2005 | ST. PAUL PIONEER PRESS
it kept selling the old devicesThe fallout from Guidant Corp.'s handling of its potentially defective Prizm 2 defibrillator intensified Thursday....

FDA INVESTIGATION OF GUIDANT CORP. PROCEEDING

May 26, 2005 | www.Newsinferno.com
Guidant has confirmed that it is "working with the FDA" regarding the agency’s investigation of Guidant’s belated admission concerning its...

Defibrillator-Maker Kept Silent About Defect

May 25, 2005 | AP
The maker of an internal heart defibrillator is acknowledging it waited three years before telling some 24,000 patients and their doctors about an...

Guidant Confirms It's Working Qith FDA on Defibrillator Problem

May 25, 2005 | AP
Medical device maker Guidant Corp. confirmed Wednesday that it is cooperating with the Food and Drug Administration as the agency looks into why...

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Guidant Defibrillators
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