Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K200112 |
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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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Biolox Ceramic Option Head Zimmer 12/14 40mm +0, Item Number 00-8777-040-02 | 2 | 12/18/2023 | Biomet, Inc. |
Biolox Ceramic Option Head Zimmer 12/14 40mm -3, Item Number 00-8777-040-01 | 2 | 12/18/2023 | Biomet, Inc. |
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