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U.S. Department of Health and Human Services

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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Aeroset Analyzer, item 9D05-01 2 05/20/2003 FEI # 1628664
Abbott Laboratories, Inc
The following brand name labeled products are under recall (all catalog numbers and all lot number... 2 05/21/2003 FEI # 1000132332
Nipro Corp
Interax Knee Midi 1 Tibial Inserts. Interax Tib Ins Midi 1 8mm Lft. 2 05/21/2003 FEI # 3003070421
Stryker Howmedica Osteonics
Interax Knee Midi 1 Tibial Inserts. Interax Tib Ins Midi 1 10mm Lft. 2 05/21/2003 FEI # 3003070421
Stryker Howmedica Osteonics
Interax Knee Midi 1 Tibial Inserts. IX HC Tib Bear Ins M1 14mm R. 2 05/21/2003 FEI # 3003070421
Stryker Howmedica Osteonics
Interax Knee Midi 1 Tibial Inserts. IX HC Tib Ins Midi 1 10mm L. 2 05/21/2003 FEI # 3003070421
Stryker Howmedica Osteonics
Interax Knee Midi 1 Tibial Inserts. IX HC Tib Ins Midi 1 14mm L. 2 05/21/2003 FEI # 3003070421
Stryker Howmedica Osteonics
Interax Knee Midi 1 Tibial Inserts. IX HC Tib Ins Midi 1 14mm R. 2 05/21/2003 FEI # 3003070421
Stryker Howmedica Osteonics
Interax Knee Midi 1 Tibial Inserts. Interax Tib Ins Midi 1 6mm Lft. 2 05/21/2003 FEI # 3003070421
Stryker Howmedica Osteonics
Interax Knee Midi 1 Tibial Inserts. Interax Tib Ins Midi 1 10 Rgt. 2 05/21/2003 FEI # 3003070421
Stryker Howmedica Osteonics

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