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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 31 Results
Recall Date to: 09/02/2014 PMA Number: P010012
 
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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, H173, H175), CONTAK RENEWAL 3 HE (models H177, H179) CONTAK ... 2 07/04/2006 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
CONTAK RENEWAL 4 CRT-D (model no. H190, H195, H199). Cardiac Resynchronization Therapy Defibrillat... 3 05/23/2006 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 3 RF (models H210, H215), CONTAK RENEWAL 3 RF HE (models H217, H219), CONTAK RENEWAL ... 3 05/16/2006 Guidant Corporation
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 (models H170,H175) CONTAK RENEWAL 3 HE (models H177, H179) Cardiac Resynchr... 2 05/02/2006 Guidant Corporation
CONTAK RENEWAL 3 DS HE, model H177 CRT-D Cardiac Resynchronization Therapy Defibrillator. Content... 2 08/03/2005 Guidant Corporation
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