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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 12 Results
Related Medical Device Recalls
 
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Product Description
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Z-1621-2024 - TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-44B 2 04/25/2024 Howmedica Osteonics Corp.
Z-1622-2024 - TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-48D 2 04/25/2024 Howmedica Osteonics Corp.
Z-1623-2024 - TRIDENTII HEMI CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-50D 2 04/25/2024 Howmedica Osteonics Corp.
Z-1624-2024 - TRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-52E 2 04/25/2024 Howmedica Osteonics Corp.
Z-1625-2024 - TRIDENTII HEMI CLUSTER54E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-54E 2 04/25/2024 Howmedica Osteonics Corp.
Z-1626-2024 - TRIDENTII HEMI CLUSTER58F- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-58F 2 04/25/2024 Howmedica Osteonics Corp.
Z-1627-2024 - TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-66H 2 04/25/2024 Howmedica Osteonics Corp.
Z-1628-2024 - TRIDENTII PSL CLUSTER48D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-48D 2 04/25/2024 Howmedica Osteonics Corp.
Z-1629-2024 - TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-50D 2 04/25/2024 Howmedica Osteonics Corp.
Z-1630-2024 - TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-52E 2 04/25/2024 Howmedica Osteonics Corp.
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