Medical Device Recalls
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1 result found
510(K) Number: K143393 |
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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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Stryker Orthopaedics Modular Handle Triathlon Instruments, Non-Sterile, REF 6541-4-808, Lot 123, NDC... | 2 | 08/09/2016 | Stryker Howmedica Osteonics Corp. |
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