Medical Device Recalls
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1 result found
PMA Number: P010012/S002 |
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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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