Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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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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Z-1750-2008 - Omnifit EON Surgical Protocol; Literature Number: LSP48 4/04 Stryker Howmedica Osteonics Corp., Mahwah, NJ | 2 | 08/17/2008 | Stryker Howmedica Osteonics Corp. |
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