Medical Device Recalls
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1 result found
510(K) Number: K915526 |
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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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AutoSuture SURGIPRO Polyproylene Mesh Clear 3" x 5" Sterile REF SPM 35 Surgipro Flat Sheet me... | 2 | 02/01/2011 | Covidien LP |
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