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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 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 DS DR/VR (Models T125, T135), Guidant VITALITY EL (Model T127), Guidant VITALITY DR... 2 11/24/2007 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 VENTAK PRIZM VR (model 1860) and VENTAK PRIZM DR (model 1861) Automatic Implantable Cardiove... 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
VITALITY HE (model T180) Implantable Cardioverter Defibrillator (ICD). Sterile EO. Guidant Corporat... 2 07/04/2006 Guidant Corporation
VITALITY DS (model T125) and VITALITY 2 (models T165, 175) ICD (implantable cardiac defibrillator) 3 05/23/2006 Guidant Corporation
Guidant VITALITY HE Implantable Cardioverter Defibrillator (model T180). Sterile EO. Guidant Corpo... 2 05/02/2006 Guidant Corporation
VITALITY AVT, model A135 and A155. Implantable Cardioverter Defibrillator. Atrial and Ventricular ... 1 08/16/2005 Boston Scientific CRM Corp
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