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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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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
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2
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01/31/2024
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Howmedica Osteonics Corp.
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Z-0910-2024 - LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT
Intended for knee replacement.
Product Number: 6637-0-631
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2
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01/31/2024
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Howmedica Osteonics Corp.
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Z-0911-2024 - RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT
Intended for knee replacement
Product Number: 6637-0-831
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2
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01/31/2024
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Howmedica Osteonics Corp.
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Z-0912-2024 - RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT
Intended for knee replacement
Product Number: 6637-0-928
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2
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01/31/2024
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Howmedica Osteonics Corp.
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Z-0913-2024 - RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT
Intended for knee replacement.
Product Number: 6637-0-931
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2
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01/31/2024
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Howmedica Osteonics Corp.
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Z-0914-2024 - PRIMARY REV.TIB.INSERT-DURACON
Intended for knee replacement.
Product Number: 6637-4-031
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2
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01/31/2024
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Howmedica Osteonics Corp.
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Z-0915-2024 - LARGE PRIMARY REV.TIB.INSERT- DURACON
Intended for knee replacement
Product Number: 6637-4-231
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2
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01/31/2024
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Howmedica Osteonics Corp.
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Z-0916-2024 - DURATION A-P LIPPED TIB.INSERT-DURAC
Intended for knee replacement
Product Number: 6642-1-709
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2
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01/31/2024
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Howmedica Osteonics Corp.
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Z-0917-2024 - DURATION A-P LIPPED TIB.INSERT-DURAC
Intended for knee replacement
Product Number: 6642-1-911
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2
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01/31/2024
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Howmedica Osteonics Corp.
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Z-0918-2024 - DURATION PLASTIC PATELLA-DURACON
Intended for knee replacement
Product Number: 6642-2-200
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2
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01/31/2024
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Howmedica Osteonics Corp.
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