Medical Device Recalls
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31 to 31 of 31 Results
Recall Date to: 09/21/2014 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 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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