Medical Device Recalls
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1 result found
510(K) Number: K041632 |
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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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Coloplast, Restorelle DirectFix, Posterior Polypropylene Mesh, Catalogue Number 501460, Rx Only, Ma... | 3 | 05/02/2012 | Coloplast Manufacturing US, LLC |
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