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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
Related Medical Device Recalls
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Z-0825-06 - Guidant CONTAK RENEWAL 3 (models H170,H175) CONTAK RENEWAL 3 HE (models H177, H179) Cardiac Resynchronization Therapy Defibrillator (CRT-D). Sterile EO. Guidant Corporation, 4100 Hamline Avenue Nort... 2 05/02/2006 FEI # 2124215
Guidant Corporation
Z-0828-06 - Guidant VITALITY HE Implantable Cardioverter Defibrillator (model T180). Sterile EO. Guidant Corporation, Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 USA. This I... 2 05/02/2006 FEI # 2124215
Guidant Corporation
Z-0827-06 - Guidant CONTAK RENEWAL 4 AVT (model M170). Cardiac Resynchronization Therapy Defibrillator (CRT-D). Sterile EO. Guidant Corporation, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 USA. Cardi... 2 05/02/2006 FEI # 2124215
Guidant Corporation
Z-0826-06 - Guidant CONTAK RENEWAL 4 (models H190, H195) CONTAK RENEWAL; 4 HE (model H197). Cardiac Resynchronization Therapy Defibrillator (CRT-D). Sterile EO. Guidant Corporation, 4100 Hamline Avenue North, ... 2 05/02/2006 FEI # 2124215
Guidant Corporation
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