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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 58 Results
Related Medical Device Recalls
 
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Product Description
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FDA Recall
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Z-0920-2024 - DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-611 2 01/31/2024 Howmedica Osteonics Corp.
Z-0919-2024 - DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-609 2 01/31/2024 Howmedica Osteonics Corp.
Z-0922-2024 - DUR PCA MTK REV INS RT Intended for knee replacement Product Number: 6728-2-711 2 01/31/2024 Howmedica Osteonics Corp.
Z-0921-2024 - DUR PCA MTK REV INS RT Intended for knee replacement Product Number: 6728-2-709 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.
Z-0901-2024 - HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee replacement Part Number: 620-00-28J 2 01/31/2024 Howmedica Osteonics Corp.
Z-0903-2024 - HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee replacement Part Number: 620-00-32J 2 01/31/2024 Howmedica Osteonics Corp.
Z-0902-2024 - HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee replacement Part Number: 620-00-32J 2 01/31/2024 Howmedica Osteonics Corp.
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