Medical Device Recalls
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1 result found
Recall Number: Z-0419-2026 |
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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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| Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 46 mm O.D., Size ... | 2 | 11/03/2025 |
FEI # 1000220733 Zimmer, Inc. |
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