Trident X3 Insert 723-10-36GRecalls & reported problems
Howmedica Osteonics Corp. · Trident X3 10 Degree Polyethylene Insert · Class 2 · Implant
All models of Trident X3 Insert (22)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07613327339512), received between Jul 26, 2022 and Jan 24, 2025 — classified as 5 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (3 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Device Dislodged or Dislocated3
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Joint Dislocation3
- Unspecified Infection2
- Insufficient Information1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryJan 24, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THIS REPORT IS FOR THE FIRST WASHOUT. I BELIEVE THIS WAS THE SECOND REVISION AS THE SURGEON MENTIONED ANOTHER WASHOUT PRIOR TO THIS, HOWEVER I¿M UNSURE OF WHEN OR WHERE THIS WAS DONE. THE SURGEON SEEMED TO THINK THIS WAS DONE AROUND THE (B)(6) 2024.
Patient problems: Insufficient Information; Unspecified Infection
MAUDE report 21230155 ↗InjurySep 18, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED DUE TO INFECTION. A WASHOUT WITH HEAD/ LINER EXCHANGE WAS PERFORMED. REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.
Patient problems: Unspecified Infection
MAUDE report 17770461 ↗InjurySep 13, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
AS REPORTED: "PLEASE FIND ATTACHED INFORMATION FROM INDEX AND REVISION PROCEDURES OF A RIGHT TOTAL HIP. THE REVISION TODAY WAS SECONDARY TO DISLOCATION. NO FURTHER INFORMATION IS AVAILABLE FROM THE DOCTOR OR HOSPITAL." SPOKE TO REP, WHO CONFIRMED THE FEMORAL HEAD DISLOCATED FROM THE LINER.
Patient problems: Joint Dislocation
MAUDE report 17735253 ↗InjuryApr 4, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
LEFT TOTAL HIP. THE REVISION TODAY WAS SECONDARY TO DISLOCATION. NO FURTHER INFORMATION IS AVAILABLE FROM THE DOCTOR OR HOSPITAL.
Patient problems: Joint Dislocation
MAUDE report 16671884 ↗InjuryJul 26, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT RETURNED TO THEATRE FOLLOWING PRIMARY HIP JOINT REPLACEMENT DUE TO HEAD DISLOCATED OUT OF LINER (SAME DAY). CUP REPOSITIONED, 10 DEG LINER EXCHANGED FOR MDM, HEAD REVISED TO ORTHINOX HEAD AND ACCOLADE II STEM REMAINED.
Patient problems: Joint Dislocation
MAUDE report 15108111 ↗
Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices
- PINNACLE 1217-25-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED735 reports
- NA 1365-52-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED683 reports
- APEX 1246-03-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 deaths613 reports
- PINNACLE 1217-20-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 deaths590 reports
- PINNACLE 1217-30-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 death484 reports
- NA 1365-53-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED404 reports
- PINNACLE ALTRX 1221-36-054Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED388 reports
- PINNACLE ALTRX 1221-32-050Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED386 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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