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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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Class
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FDA Recall
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Recalling Firm
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VITEK 2 - AST Test kits (in vitro diagnostic test cards for antimicrobial susceptibility): a) AST... 1 04/25/2024 Biomerieux Inc
Baxter Seprafilm Adhesion Barrier 1 Half Sheet, 5-PK, REF 664103, for use in abdominal and pelvic su... 2 04/25/2024 Baxter Healthcare Corporation
TRIDENTII HEMI CLUSTER54E- Indicated for use in primary and revision patients at high risk of hip d... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision patients at high risk of hip dis... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip disl... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision patients at high risk of hip dis... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dis... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision patients at high risk of hip d... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dis... 2 04/25/2024 Howmedica Osteonics Corp.
TRIDENTII HEMI CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip di... 2 04/25/2024 Howmedica Osteonics Corp.

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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