Trident 540-11-52ERecalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 04546540237835), received between Sep 14, 2018 and Apr 15, 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.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryApr 15, 2026Noise, Audible

  THE FOLLOWING INFORMATION WAS PROVIDED: PATIENT REPORTED SQUEAKING WHEN MOVING HIP. PATIENT SENT FOR X-RAY AND SCANS FOR IMPLANT PLANNING. SURGEON SCHEDULES PATIENT FOR REVISION SURGERY TO REPLACE/REPOSITION CUP. OLD CUP, LINER AND FEMORAL HEADS REMOVED. HEAVY WEAR NOTED ON FEMORAL HEAD AND LINER. ALL COMPONENTS IN SITU (EXCEPT STEM) ARE REPLACED.

  Patient problems: Insufficient Information

  MAUDE report 24885752 ↗
• InjuryMar 12, 2024Degraded; Adverse Event Without Identified Device or Use Problem; Degraded; Adverse Event Without Identified Device or Use Problem

  RIGHT HIP REVISION PROCEDURE. CAUSE OF REVISION WAS PSEUDOTUMOUR. ALL PRIMARY IMPLANTS WERE REMOVED AND REPLACED BY A PROXIMAL FEMUR GMRS, CEMENTED CONSTRAINED LINER AND ACETABULAR CAGE OF COMPETITOR PRODUCT.

  Patient problems: Foreign Body Reaction; Insufficient Information

  MAUDE report 18891631 ↗
• InjuryJun 28, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THE PATIENT'S RIGHT HIP WAS REVISED AFTER PATIENT COMPLAINT OF GROIN PAIN AND LIMITED ROM. A SHELL, LINER, AND FEMORAL HEAD WERE REVISED. REP CONFIRMED THAT NOTHING WAS NOTED TO BE BROKEN OR LOOSE INTRA-OPERATIVELY, AND THAT NO FURTHER INFORMATION WILL BE RELEASED BY THE HOSPITAL OR SURGEON.

  Patient problems: Loss of Range of Motion; Pain

  MAUDE report 17222204 ↗
• InjuryJun 7, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT'S LEFT HIP WAS REVISED. APPROXIMATELY 8 WEEKS PRIOR TO REVISION, PATIENT FELL AND SUSTAINED AN ACETABULAR FRACTURE. SURGEON DECIDED TO LET THE FRACTURE HEAL, THEN REVISED THE PATIENT'S SHELL, LINER, AND HEAD. REP CONFIRMED THAT THERE ARE NO ALLEGATIONS AGAINST THE REVISED HEAD AND LINER.

  Patient problems: Bone Fracture(s); Fall

  MAUDE report 14617287 ↗
• InjuryJun 29, 2020Device Dislodged or Dislocated; Insufficient Device Problem Information; Device Dislodged or Dislocated; Insufficient Device Problem Information

  LOOSE ACCOLADE TMZF FEMORAL STEM WITH MIS POSITIONED ACETABULAR LINER WITH ALUMINA CERAMIC IN CERAMIC BEARING. CORRECTION 15/JUNE/2020 WG: SPOKE TO REP. THE SHELL WAS MALPOSITIONED, NOT THE ALUMINA LINER.

  Patient problems: Ambulation or Postural Difficulties; Injury

  MAUDE report 10206333 ↗
• InjurySep 14, 2018Device Dislodged or Dislocated; Device Dislodged or Dislocated

  LINER DISLOCATION AFTER ONE MONTH OF IMPLANTATION. THE LINER WAS REVISED. UPDATE FROM REP: LINER DISLOCATED FROM SHELL.

  Patient problems: Injury

  MAUDE report 7876477 ↗