Trident 623-00-32BRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327025293), received between Mar 27, 2019 and Feb 19, 2021 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Material Deformation” (1 report).

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

• MalfunctionFeb 19, 2021Material Deformation; Material Deformation

  THE FOLLOWING WAS REPORTED: X3 LINER WAS IMPACTED AS USUAL. WHEN THE SURGEON CHECKED STABILITY WITH ELEVA, IT MADE A SLIGHT BENDING MOVEMENT ON ONE SIDE. SURGEON CHECKED AGAIN, BUT IT DIDN'T CHANGE. IN THE END, IT DIDN'T COME OFF, SO PROCEDURE WAS COMPLETED. WHEN SUCH AN EVENT OCCURS, WHAT COULD BE HAPPENED? ARE THERE ANY SIMILAR EVENT ?

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11347963 ↗
• InjuryMar 27, 2019Use of Device Problem; Use of Device Problem

  IT WAS REPORTED THAT THE PATIENT'S RIGHT HIP WAS REVISED. AS REPORTED BY REP: "PREOPERATIVE DIAGNOSIS: RIGHT FAILED TOTAL HIP ARTHROPLASTY, COMPLICATION OF PROSTHETIC HIP IMPLANT¿[SURGEON] COMMENTED NO BONY INGROWTH TO CUP, ONLY FIBROUS¿" A SHELL, SCREW, INSERT, AND HEAD WERE REVISED. ON 27-FEB-2019: MEDICAL REVIEW WAS RECEIVED WHICH IDENTIFIED BONY IMPINGEMENT BETWEEN ACETABULUM AND FEMORAL STEM, ACETABULAR COMPONENT MALPOSITION AND INAPPROPRIATE SELECTION REGARDING THE TRIDENT LINER

  Patient problems: Inadequate Osseointegration; Injury

  MAUDE report 8457162 ↗