Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K032163 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product Number: 6642... | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
DURATION PLASTIC PATELLA-DURACON Intended for knee replacement Product Number: 6642-2... | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product Number: 6642... | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
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