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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 36 Results
PMA Number: P010012
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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
VITALITY DR HE Implantable Cardioverter Defibrillator (model T180). Sterile EO. Guidant Corporation... 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
Guidant CONTAK RENEWAL 3 AVT (models M150, M155), CONTAK RENEWAL 3 AVT HE (models M157, M159), CONTA... 2 07/04/2006 Guidant Corporation
Guidant CONTAK RENEWAL 3 (models H170, H173, H175), CONTAK RENEWAL 3 HE (models H177, H179) CONTAK ... 2 07/04/2006 Guidant Corporation
CONTAK RENEWAL 3 CRT-D (model no. H170, H175, H177, H179). Cardiac Resynchronization Therapy Defibr... 3 05/23/2006 Guidant Corporation
CONTAK RENEWAL 4 CRT-D (model no. H190, H195, H199). Cardiac Resynchronization Therapy Defibrillat... 3 05/23/2006 Guidant Corporation
CONTAK RENEWAL 3 RF (models H210, H215), CONTAK RENEWAL 3 RF HE (models H217, H219), CONTAK RENEWAL ... 3 05/16/2006 Guidant Corporation
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