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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 29 Results
Recall Date to: 08/27/2014 PMA Number: P960040
 
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VITALITY DS (model T125) and VITALITY 2 (models T165, 175) ICD (implantable cardiac defibrillator) 3 05/23/2006 Guidant Corporation
Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models... 2 10/17/2013 Boston Scientific CRM Corp
Boston Scientific, ENERGEN DR ICD, Model E143. The device is an Implantable Cardioverter Defibrillat... 2 08/16/2013 Boston Scientific CRM Corp
Guidant, Vitality HE ICD, Model: T180DDR, Sterile Lot, Guidant Corporation, Cardiac Rhythm Managemen... 2 10/07/2010 Boston Scientific CRM Corp
Boston Scientific CONFIENT, model E030, Implantable Cardioverter Defibrillator (ICD). The CONFIENT ... 2 05/08/2010 Boston Scientific CRM Corp
VITALITY Implantable Cardioverter Defibrillator. Atrial and Ventricular Therapies. AVT, model A1... 2 05/08/2010 Boston Scientific CRM Corp
Boston Scientific TELIGEN, Implantable Cardiac Defibrillator, Models E102 and E110. Sterilized using... 2 05/08/2010 Boston Scientific CRM Corp
VENTAK PRIZM Automatic Implantable Cardioverter Defibrillator (AICD). DR, model 1851, DR HE, model ... 2 05/08/2010 Boston Scientific CRM Corp
Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models... 2 01/13/2010 Boston Scientific CRM Corp
Boston Scientific TELIGEN, Implantable Cardiac Defibrillator, Models E102 and E110. Sterilized usin... 2 08/18/2009 Boston Scientific CRM Corp
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