Medical Device Recalls
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31 to 31 of 31 Results
Recall Date to: 09/02/2014 PMA Number: P010012 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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CONTAK RENEWAL (model H135) Heart Failure Device Cardiac Resynchronization Therapy Defibrillators (C... | 1 | 06/30/2005 | Guidant Corporation |
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