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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 30 Results
Recall Date to: 10/04/2015 PMA Number: P960040
 
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VENTAK PRIZM AVT model no. 1900, Atrial and Ventricular Therapies. Sterilized using gaseous ethylen... 1 08/16/2005 Boston Scientific CRM Corp
VITALITY AVT, model A135 and A155. Implantable Cardioverter Defibrillator. Atrial and Ventricular ... 1 08/16/2005 Boston Scientific CRM Corp
Ventak PRIZM 2 DR, model 1861 Automatic Implantable Cardioverter Defibrillator (AICD), Dual Chamber,... 1 06/30/2005 Guidant Corporation
Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models... 2 10/18/2014 Boston Scientific CRM Corp
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 TELIGEN, Implantable Cardiac Defibrillator, Models E102 and E110. Sterilized using... 2 05/08/2010 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
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