Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K190656 |
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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., 44 mm O.D., Size ... | 2 | 11/03/2025 | Zimmer, Inc. |
| Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 46 mm O.D., Size ... | 2 | 11/03/2025 | Zimmer, Inc. |
| Dual Mobility Vivacit-E Bearing, Model Number 110031009 | 2 | 10/06/2020 | Zimmer Biomet, Inc. |
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