Medical Device Recalls
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1 result found
510(K) Number: K063633 |
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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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| Universal Femoral Sleeves - Product Usage: used primarily in revision surgeries with the S-ROM Noile... | 2 | 02/09/2021 |
FEI # 1818910 DePuy Orthopaedics, Inc. |
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