Medical Device Recalls
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1 result found
510(K) Number: K122440 |
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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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| Rostorelle L, Polypropylene Mesh, Catalog number 501440, Manufacturer Coloplast A/S 3050 Denmark. | 2 | 05/20/2013 |
FEI # 2125050 Coloplast Manufacturing US, LLC |
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