Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K171768 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip disl... | 2 | 04/25/2024 | Howmedica Osteonics Corp. |
TRIDENTII HEMI CLUSTER58F- Indicated for use in primary and revision patients at high risk of hip di... | 2 | 04/25/2024 | Howmedica Osteonics Corp. |
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