Medical Device Recalls
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1 result found
510(K) Number: K092032 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Bard® PerFix Light Plug The Bard® PerFix Light Plug is indicated for reinforcement if soft tiss... | 2 | 11/07/2014 | Davol, Inc., Subs. C. R. Bard, Inc. |
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