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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 8 of 8 Results
Related Medical Device Recalls
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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-0851-03 - Interax Knee Midi 1 Tibial Inserts. Interax Tib Ins Midi 1 6mm Lft. 2 05/21/2003 Stryker Howmedica Osteonics
Z-0852-03 - Interax Knee Midi 1 Tibial Inserts. Interax Tib Ins Midi 1 8mm Lft. 2 05/21/2003 Stryker Howmedica Osteonics
Z-0853-03 - Interax Knee Midi 1 Tibial Inserts. Interax Tib Ins Midi 1 10mm Lft. 2 05/21/2003 Stryker Howmedica Osteonics
Z-0858-03 - Interax Knee Midi 1 Tibial Inserts. IX HC Tib Ins Midi 1 14mm R. 2 05/21/2003 Stryker Howmedica Osteonics
Z-0855-03 - Interax Knee Midi 1 Tibial Inserts. Interax Tib Ins Midi 1 10 Rgt. 2 05/21/2003 Stryker Howmedica Osteonics
Z-0856-03 - Interax Knee Midi 1 Tibial Inserts. IX HC Tib Ins Midi 1 10mm L. 2 05/21/2003 Stryker Howmedica Osteonics
Z-0857-03 - Interax Knee Midi 1 Tibial Inserts. IX HC Tib Ins Midi 1 14mm L. 2 05/21/2003 Stryker Howmedica Osteonics
Z-0854-03 - Interax Knee Midi 1 Tibial Inserts. IX HC Tib Bear Ins M1 14mm R. 2 05/21/2003 Stryker Howmedica Osteonics
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