Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K020381 |
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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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RED SEXP DSTL FEM 19CM LT ASSY, model # CP111828 | 2 | 12/29/2017 | Zimmer Biomet, Inc. |
RED SEXP DSTL FEM 19CM RT ASSY, model # CP111817 | 2 | 12/29/2017 | Zimmer Biomet, Inc. |
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