Medical Device Recalls
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31 to 36 of 36 Results
PMA Number: P010012 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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 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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