Medical Device Recalls
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31 to 32 of 32 Results
Recall Date to: 09/01/2015 PMA Number: P010012 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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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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