Medical Device Recalls
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31 to 36 of 36 Results
PMA Number: P010012 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Guidant CONTAK RENEWAL 4 AVT (model M170). Cardiac Resynchronization Therapy Defibrillator (CRT-D)... | 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 |
Guidant CONTAK RENEWAL 4 (models H190, H195) CONTAK RENEWAL; 4 HE (model H197). Cardiac Resynchroni... | 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 |
CONTAK RENEWAL 3 CRT-D (model no. H170, H173, H175) and CONTAK RENEWAL 3 HE CRT-D(model no. H177 and... | 2 | 06/30/2005 | Guidant Corporation |
CONTAK RENEWAL (model H135) Heart Failure Device Cardiac Resynchronization Therapy Defibrillators (C... | 1 | 06/30/2005 | Guidant Corporation |
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