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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: 01/28/2015 PMA Number: P960040
 
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Ventak PRIZM 2 DR, model 1861 Automatic Implantable Cardioverter Defibrillator (AICD), Dual Chamber,... 1 06/30/2005 Guidant Corporation
VENTAK PRIZM AVT model no. 1900, Atrial and Ventricular Therapies. Sterilized using gaseous ethylen... 2 06/30/2005 Boston Scientific CRM Corp
VITALITY AVT, model A135 and model A155. Implantable Cardioverter Defibrillator. Atrial and Ventr... 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
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
Guidant VITALITY HE Implantable Cardioverter Defibrillator (model T180). Sterile EO. Guidant Corpo... 2 05/02/2006 Guidant Corporation
VITALITY DS (model T125) and VITALITY 2 (models T165, 175) ICD (implantable cardiac defibrillator) 3 05/23/2006 Guidant Corporation
VITALITY HE (model T180) Implantable Cardioverter Defibrillator (ICD). Sterile EO. Guidant Corporat... 2 07/04/2006 Guidant Corporation
VITALITY AVT, model A155. Implantable Cardioverter Defibrillator. Atrial and Ventricular Therapies. ... 2 07/27/2006 Boston Scientific CRM Corp
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