Trident X3 Insert 723-10-32DRecalls & 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
- 6
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 07613327339383), received between Oct 18, 2021 and May 27, 2026 — classified as 6 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. 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
- Adverse Event Without Identified Device or Use Problem3
- Device Dislodged or Dislocated2
- Insufficient Device Problem Information1
Patient problems
- Unspecified Infection4
- Joint Dislocation2
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryMay 27, 2026Adverse Event Without Identified Device or Use Problem
THE FOLLOWING INFORMATION WAS PROVIDED: IT WAS REPORTED THAT: INFECTION.
Patient problems: Unspecified Infection
MAUDE report 25304477 ↗InjuryOct 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJul 19, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED BY SALES REPRESENTATIVE THAT PATIENT DID A LEFT MAKO PRIMARY THA ON (B)(6)2024. CASE WENT WELL. HOWEVER, PATIENT HAD SUFFERED A STROKE AND WAS SENT TO ICU. DURING A&E HANDLING, HER LEFT HIP GOT DISLOCATED. WHILE DR. TRIED TO RELOCATE THE HIP FOR PATIENT UNDER GA, FEMORAL STEM CAME OUT FROM CANAL. REVISION SURGERY IS PLANNED.
Patient problems: Joint Dislocation
MAUDE report 19785546 ↗InjuryJun 26, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
AS REPORTED: "DR. REVISED A RIGHT HIP DUE TO DISLOCATION." REP CONFIRMED THE FEMORAL HEAD DISLOCATED OUT OF THE POLY LINER.
Patient problems: Joint Dislocation
MAUDE report 17206054 ↗InjuryFeb 22, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
AS REPORTED: "THIS RIGHT HIP WAS REVISED DUE TO POSSIBLE INFECTION. HEAD AND LINER SWAP ONLY." PATIENT WAS REVISED FROM A 32D POLY INSERT AND 32 -4MM V40 HEAD NEW DEVICES OF THE SAME TYPE AND SIZE.
Patient problems: Unspecified Infection
MAUDE report 13577871 ↗InjuryOct 18, 2021Insufficient Device Problem Information; Insufficient Device Problem Information
AS REPORTED: "PATIENT REVISED HEAD AND LINER DUE TO POSSIBLE INFECTION. RIGHT HIP. NO OTHER INFORMATION AVAILABLE DUE TO THE HOSPITAL POLICY." SPOKE TO REP, WHO SUPPLIED THE PRIMARY AND REVISION USAGE. NO RELEASE OF EXPLANTS, AND NO FURTHER INFORMATION DUE TO HOSPITAL POLICY.
Patient problems: Unspecified Infection
MAUDE report 12646486 ↗
Other Prosthesis, hip, constrained, cemented or uncemented, metal/polymer devices
- Novation 134-36-45Exactech, Inc. · Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer2 recalls0 reports
- PINNACLE 1218-28-650Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer89 reports
- Trident 690-00-28FHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall37 reports
- Trident 690-00-22EHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall36 reports
- PINNACLE 1218-32-652Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer75 reports
- Trident 690-00-22DHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall22 reports
- PINNACLE 1218-32-654Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer70 reports
- Trident 69-2850Howmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall11 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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