InjuryJDI
TRIDENT HEMI CLUSTER HOLE SHELL
Received Jul 15, 2026 · Event occurred Jun 19, 2026
Report 0002249697-2026-00627 · MDR key 25833606
Device
Generic name
Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented
Manufacturer
Stryker Orthopaedics-mahwahCatalog number
502-11-60G
Lot number
97059901
Product problems
- Loss of Osseointegration
Patient
NA · Unknown
- Inadequate Osseointegration
Narrative
Additional Manufacturer Narrative
REVIEW OF THE DEVICE HISTORY RECORDS INDICATE THAT DEVICES WERE MANUFACTURED AND ACCEPTED INTO FINAL STOCK WITH NO REPORTED DISCREPANCIES. THERE HAVE BEEN NO OTHER EVENTS FOR THE LOT REFERENCED. IF ADDITIONAL INFORMATION IS RECEIVED, IT WILL BE PROVIDED IN A SUPPLEMENTAL REPORT UPON COMPLETION OF THE INVESTIGATION.
Description of Event or Problem
THE FOLLOWING INFORMATION WAS PROVIDED: TRIDENT LEGACY CUP REVISION. CUP HAD ABSOLUTELY NO BONE INTEGRATION ONLY STAYING IN BY 1 SCREW.