Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K040770 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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various polyethylene implants Knees Revision Tibial Tray Systems Oxford Partial Knee Orthopedic... | 2 | 03/27/2017 | Zimmer Biomet, Inc. |
Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764 | 2 | 02/23/2019 | Zimmer Biomet, Inc. |
Knee Products: 184762 Knees Vanguard Knee System, Series-A Standard Patella, 28 MM; 184764 Knees... | 2 | 05/28/2020 | Biomet, Inc. |
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