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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 40 of 58 Results
Related Medical Device Recalls
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Product Description
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Z-0871-2024 - SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0030 2 01/31/2024 Howmedica Osteonics Corp.
Z-0870-2024 - SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0028 2 01/31/2024 Howmedica Osteonics Corp.
Z-0869-2024 - SCORPIO RECESSED PATELLA- Intended for Knee Replacement Part Number: 3044-0026 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-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-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-0925-2024 - PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-416 2 01/31/2024 Howmedica Osteonics Corp.
Z-0923-2024 - PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-411 2 01/31/2024 Howmedica Osteonics Corp.
Z-0924-2024 - PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-413 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.
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