Medical Device Recalls
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1 result found
Recall Number: Z-0873-2016 |
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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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| Stryker, T2 K-Wire, 3x285 mm Product Usage: Intended for the temporary stabilization of bone seg... | 2 | 02/25/2016 |
FEI # 3003070421 Stryker Howmedica Osteonics Corp. |
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