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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 35 Results
PMA Number: P960040
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Guidant VITALITY DS DR/VR (Models T125, T135), Guidant VITALITY EL (Model T127), Guidant VITALITY DR... 2 11/24/2007 Boston Scientific CRM Corp
Guidant VITALITY 2 DR/VR (Models T165, T175) and Guidant VITALITY 2 EL DR/VR (Models T167, T177). I... 2 11/24/2007 Boston Scientific CRM Corp
Guidant VITALITY 2 (models T165, T175), VITALITY DS (model T125), VITALITY EL (model T135), Implant... 2 07/27/2006 Boston Scientific CRM Corp
Guidant VENTAK PRIZM VR (model 1860) and VENTAK PRIZM DR (model 1861) Automatic Implantable Cardiove... 2 09/28/2006 Boston Scientific CRM Corp
GUIDANT VITALITY® DS VR Model T135 VR; EL Model T127 DR; 2ICD Model T165 DR; 2ICD Model T175 VR; 2E... 2 07/17/2009 Boston Scientific CRM Corp
Boston Scientific, Implantable Cardioverter Defibrillator, DYNAGEN EL ICD DR, Model D152 - Product U... 2 03/03/2020 Boston Scientific Corporation
Boston Scientific, ENERGEN DR ICD, Model E143. The device is an Implantable Cardioverter Defibrillat... 2 08/16/2013 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 TELIGEN, Implantable Cardiac Defibrillator, Models E102 and E110. Sterilized usin... 2 08/18/2009 Boston Scientific CRM Corp
Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models... 2 10/17/2013 Boston Scientific CRM Corp
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