TRIDENTII HEMI hip implant recalled for acetabular shell manufacturing defect
Howmedica Osteonics is recalling the TRIDENTII HEMI CLUSTER48D hip implant because the acetabular shell may have excessive deburring, resulting in a smooth surface on the shell edge.
- Product
- TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-48D
- Category
- Medical Device
- Distribution
- Distributed nationwide