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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 30 Results
Recall Date to: 03/03/2015 PMA Number: P960040
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VENTAK PRIZM Automatic Implantable Cardioverter Defibrillator (AICD). DR, model 1851, DR HE, model ... 2 05/08/2010 Boston Scientific CRM Corp
VENTAK PRIZM AVT model no. 1900, Atrial and Ventricular Therapies. Sterilized using gaseous ethylen... 1 08/16/2005 Boston Scientific CRM Corp
VENTAK PRIZM AVT model no. 1900, Atrial and Ventricular Therapies. Sterilized using gaseous ethylen... 2 06/30/2005 Boston Scientific CRM Corp
PRIZM 2 DR, model 1861 Automatic Implantable Cardioverter Defibrillator. Contents have been Sterili... 2 08/03/2005 Guidant Corporation
Guidant, Vitality HE ICD, Model: T180DDR, Sterile Lot, Guidant Corporation, Cardiac Rhythm Managemen... 2 10/07/2010 Boston Scientific CRM Corp
Guidant VITALITY HE Implantable Cardioverter Defibrillator (model T180). Sterile EO. Guidant Corpo... 2 05/02/2006 Guidant Corporation
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
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