Medical Device Recalls
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1 result found
510(K) Number: K031925 |
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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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PROCEED Surgical Mesh is a sterile, thin, flexible laminate mesh designed for the repair of hernias ... | 2 | 01/26/2006 | Ethicon, Inc. |
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