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U.S. Department of Health and Human Services

Medical Device Recalls

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41 to 50 of 58 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0909-2024 - LEFT X-LARGE-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-328 2 01/31/2024 Howmedica Osteonics Corp.
Z-0910-2024 - LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-631 2 01/31/2024 Howmedica Osteonics Corp.
Z-0911-2024 - RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement Product Number: 6637-0-831 2 01/31/2024 Howmedica Osteonics Corp.
Z-0912-2024 - RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement Product Number: 6637-0-928 2 01/31/2024 Howmedica Osteonics Corp.
Z-0913-2024 - RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-931 2 01/31/2024 Howmedica Osteonics Corp.
Z-0914-2024 - PRIMARY REV.TIB.INSERT-DURACON Intended for knee replacement. Product Number: 6637-4-031 2 01/31/2024 Howmedica Osteonics Corp.
Z-0915-2024 - LARGE PRIMARY REV.TIB.INSERT- DURACON Intended for knee replacement Product Number: 6637-4-231 2 01/31/2024 Howmedica Osteonics Corp.
Z-0916-2024 - DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product Number: 6642-1-709 2 01/31/2024 Howmedica Osteonics Corp.
Z-0917-2024 - DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product Number: 6642-1-911 2 01/31/2024 Howmedica Osteonics Corp.
Z-0918-2024 - DURATION PLASTIC PATELLA-DURACON Intended for knee replacement Product Number: 6642-2-200 2 01/31/2024 Howmedica Osteonics Corp.
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