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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 29 Results
Recall Date to: 09/20/2014 PMA Number: P960040
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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 TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following model... 2 07/14/2009 Boston Scientific CRM Corp
VITALITY EL, models T127, T167, T177 Implantable Cardioverter Defibrillator (ICD), pulse-generator, ... 2 08/21/2008 Boston Scientific CRM Corp
VITALITY DR+ Implantable Cardioverter Defibrillator (ICD), model 1872 2 08/21/2008 Boston Scientific CRM Corp
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 VENTAK PRIZM VR (model 1860) and VENTAK PRIZM DR (model 1861) Automatic Implantable Cardiove... 2 09/28/2006 Boston Scientific CRM Corp
VITALITY (models 1870, 1871, T125, T127, T135) and VITALITY 2 (models T165, T167, T175, T177). Impl... 2 09/28/2006 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
VITALITY AVT, model A155. Implantable Cardioverter Defibrillator. Atrial and Ventricular Therapies. ... 2 07/27/2006 Boston Scientific CRM Corp
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