Trident X3 Insert 743-00-36ERecalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07613327342765), received between Mar 29, 2022 and Dec 11, 2024 — 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.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryDec 11, 2024Unstable; Unstable

  REVISED A LEFT HIP LINER AND HEAD DUE TO INSTABILITY.

  Patient problems: Joint Laxity

  MAUDE report 20908636 ↗
• InjuryMay 3, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED DUE TO DISLOCATION OF THE HEAD FROM THE LINER. THE HEAD AND LINER WERE REVISED TO A NEW FEMORAL HEAD, ADM/ MDM POLY INSERT, AND MDM METAL LINER.

  Patient problems: Joint Dislocation

  MAUDE report 19236839 ↗
• InjuryDec 11, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED DUE TO DISLOCATION OF A CEMENTED LINER FROM THE PATIENT'S NATIVE ACETABULUM. SURGEON REPORTED DISLOCATION OCCURRED BECAUSE THE CEMENT DID NOT INTERDIGITATE WITH THE PATIENT'S NATIVE ACETABULUM DUE TO A FRACTURE IN THE POSTERIOR ASPECT OF THE ACETABULUM (CAUSE OR DATE OF FRACTURE UNKNOWN). THE CEMENTED LINER AND FEMORAL HEAD WERE REMOVED, ORIF WAS PERFORMED, AND A GAP RING CAGE WITH SCREWS, A CEMENTED EXETER ALL-POLY CUP, AND NEW FEMORAL HEAD WERE IMPLANTED. REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Joint Dislocation

  MAUDE report 18307779 ↗
• InjuryNov 20, 2023Degraded; Degraded

  IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED DUE TO PSOAS IMPINGEMENT. INTRAOPERATIVELY, ABNORMAL WEAR WAS NOTED ON THE ELEVATED RIM OF THE LINER (EXACT CAUSE OF WEAR UNKNOWN). A SHELL, LINER AND HEAD WERE REVISED. REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Muscle/Tendon Damage

  MAUDE report 18168711 ↗
• InjuryMar 29, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  AS REPORTED: "PATIENT DISLOCATED AND WAS REVISED. CUP WAS REPOSITIONED AND CONVERTED TO AN MDM. NO ALLEGATIONS AGAINST THE IMPLANTS. ORIGINAL USAGE AND REVISION USAGE ATTACHED. NO FURTHER INFORMATION IS AVAILABLE." SPOKE TO REP. THE HEAD HAD DISLOCATED FROM THE LINER. THE ELEVATED RIM LINER AND FEMORAL HEAD WERE REVISED TO A METAL MDM LINER, ADM/ MDM POLY INSERT, AND FEMORAL HEAD WITH SLEEVE. THE SURGEON REMOVED 2 SCREWS FROM THE IN-SITU ACETABULAR SHELL, REPOSITIONED THAT SAME SHELL, REIMPLANTED THE ORIGINAL 2 SCREWS, AND ADDED AN ADDITIONAL SCREW. REP CONFIRMED THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Joint Dislocation

  MAUDE report 13944938 ↗