Trident 69-2852Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327025484), received between Oct 28, 2024 and Jun 10, 2026 — classified as 2 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Jul 30, 2026Open, Classified

   Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and inflammation.

   Z-3201-2026 · Root cause: Process change control · FDA record ↗

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJun 10, 2026Device Dislodged or Dislocated

  THE FOLLOWING WAS REPORTED: THE FIRST SURGERY WAS DONE ON (B)(6) 2026. PATIENT HAS COME BACK WITH DISLOCATION OF HIP AND REVISION WAS DONE. LEFT SIDE.

  Patient problems: Joint Dislocation

  MAUDE report 25455749 ↗
• InjuryOct 28, 2024Fracture; Fracture

  TRIDENT ALL POLY CONSTRAINED ACETABULAR INSERT HAS BEEN BROKEN WHILE IMPLANTED IN PATIENTPATIENT CAME TO THE SURGEON AFTER 2 MONTHS OF THE THR REVISED SURGERY WITH COMPLAINT OF THE HIP PAIN. SURGEON GOT HIS HIP XRAY DONE AND FOUND THAT TRIDENT CONSTRAINED ACETABULAR INSERT WAS BROKEN.

  Patient problems: Ambulation or Postural Difficulties; Pain

  MAUDE report 20553251 ↗