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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 32 Results
Recall Date to: 04/25/2015 PMA Number: P010012
 
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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 2 (model T165, T175), VITALITY DS (model T125, T135), VITALITY EL (model T127), Implantable... 2 07/11/2007 Boston Scientific CRM Corp
Guidant, CONTAK RENEWAL 3/3RF Models H170, H175, H177, H179, H210, H215, H217, H219, Guidant Corpor... 2 10/07/2010 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
Guidant Contak® Renewal® 3 CRT-D Model H170; 3CRT-D, Model H175; 3HE CRT-D, Model H177; 3HE CRT-D, M... 2 07/17/2009 Boston Scientific CRM Corp
Guidant CONTAK RENEWAL 4 AVT (model M170). Cardiac Resynchronization Therapy Defibrillator (CRT-D)... 2 05/02/2006 Guidant Corporation
Guidant CONTAK RENEWAL 4 (models H190, H195) CONTAK RENEWAL; 4 HE (model H197). Cardiac Resynchroni... 2 05/02/2006 Guidant Corporation
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 AVT (models M150, M155), CONTAK RENEWAL 3 AVT HE (models M157, M159), CONTA... 2 07/04/2006 Guidant Corporation
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