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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 31 Results
Recall Date to: 08/29/2014 PMA Number: P010012
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Guidant CONTAK RENEWAL 3 (Models H170, H173, H175), Guidant CONTAK RENEWAL 3 HE (Models H177, H179).... 2 11/24/2007 Boston Scientific CRM Corp
Guidant VITALITY VR/DR, Implantable Cardioverter Defibrillator, ICD, Models 1870 and 1871. Guidan... 2 11/24/2007 Boston Scientific CRM Corp
VITALITY AVT (model A155). Implantable Cardioverter Defibrillator. Atrial and Ventricular Therapies.... 2 07/11/2007 Boston Scientific CRM Corp
VITALITY 2 EL DR/VR (model T167, T177). contents have been sterilized with gaseous ethylene oxide. ... 2 07/11/2007 Boston Scientific CRM Corp
VITALITY DR HE Implantable Cardioverter Defibrillator (model T180). Sterile EO. Guidant Corporation... 2 07/11/2007 Boston Scientific CRM Corp
VITALITY 2 (model T165, T175), VITALITY DS (model T125, T135), VITALITY EL (model T127), Implantable... 2 07/11/2007 Boston Scientific CRM Corp
CONTAK RENEWAL 3 RF (model H210, H215), CONTAK RENEWAL 3 RF HE (model H217, H219) cardiac resynchron... 2 07/11/2007 Boston Scientific CRM Corp
CONTAK RENEWAL 3 (model H170, H175) CONTAK RENEWAL 3 HE (model H177, H179) Cardiac Resynchronization... 2 07/11/2007 Boston Scientific CRM Corp
Guidant CONTAK RENEWAL 3 RF (models H210, H215), CONTAK RENEWAL 3 RF HE (models H217, H219) ,CONTAK ... 2 12/16/2006 Guidant Corporation
Guidant CONTAK RENEWAL 3 (models H170, H175) CONTAK RENEWAL 3 HE (models H177, H179) Cardiac Resynch... 2 07/27/2006 Boston Scientific CRM Corp
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