Medical Device Recalls
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11 to 12 of 12 Results
Related Medical Device Recalls |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-1631-2024 - TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-58F | 2 | 04/25/2024 | Howmedica Osteonics Corp. |
Z-1626-2024 - TRIDENTII HEMI CLUSTER58F- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-58F | 2 | 04/25/2024 | Howmedica Osteonics Corp. |
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