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Howmedica Osteonics Corp. recalls TRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Nu
Recalled May 1, 2024 · FDA recall Z-1624-2024 · Howmedica Osteonics
Hazard
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell · FDA Class II
Units
48 units
Sold at
Nationwide Foreign: Netherlands, Canada, Singapore, Spain, Sweden, UK
Description
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
Product
TRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-52E
Manufacturer(s)
Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →