Device evidence

device-recall:cfres:206584

TRIDENTII HEMI CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-50D

Official recall number

Z-1623-2024

Evidence summary

Product code: LPH
Recall status: Open, Classified
Event initiated: February 27, 2024
Root cause: Under Investigation by firm
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-1623-2024