Trident 65C-3256Recalls & reported problems
Howmedica Osteonics Corp. · Polyethylene Acetabular Cup · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327024302), received between Aug 28, 2019 and Sep 3, 2019 — classified as 2 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Device Dislodged or Dislocated2
Patient problems
- Injury2
- Joint Dislocation2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjurySep 3, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated
THIS PI IS FOR THE REVISION DUE TO A SECOND DISLOCATION OF THE FEMORAL HEAD FROM THE ALL-POLY CUP. IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED DUE TO DISLOCATION 4 DAYS AFTER A STAGE 1 REVISION FOR INFECTION HAD BEEN PERFORMED. THE PATIENT DISLOCATED AGAIN 5 DAYS LATER AND ALL COMPONENTS (OMNIFIT HFX STEM, 32+10 C-TAPER LFIT HEAD, TRIDENT ALL POLY CUP) WERE REVISED TO AN OMNIFIT EON PLUS STEM, 28 +0 C-TAPER LFIT HEAD, AND UHR BIPOLAR COMPONENT. REP PROVIDED USAGE SHEETS FOR THE IMPLANTATION AND REVISION, AND REPORTED THAT NO FURTHER INFORMATION WILL BE AVAILABLE.
Patient problems: Injury; Joint Dislocation
MAUDE report 8955598 ↗InjuryAug 28, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated
THIS PI IS FOR THE REVISION DUE TO DISLOCATION OF THE FEMORAL HEAD FROM THE ALL-POLY CUP. IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED DUE TO DISLOCATION 4 DAYS AFTER A STAGE 1 REVISION FOR INFECTION HAD BEEN PERFORMED. A 32 +5 BIOLOX DELTA C-TAPER HEAD WAS REVISED TO A 32+10 C-TAPER LFIT HEAD (THE ALL POLY CUP WAS NOT REVISED). REP PROVIDED USAGE SHEETS FOR THE IMPLANTATION AND REVISION, AND REPORTED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.
Patient problems: Injury; Joint Dislocation
MAUDE report 8939451 ↗
Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices
- NA 1365-51-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented753 reports
- NA 1365-50-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented412 reports
- ARTICUL/EZE 1365-21-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 1365-11-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- LFIT 6260-9-236Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, cemented256 reports
- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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