Persona® Trabecular Metal® 42-5022-062-02Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024470088), received between May 20, 2022 and May 16, 2024 — classified as 4 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 18, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryMay 16, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT UNDERWENT A RIGHT KNEE REVISION APPROXIMATELY TWO MONTHS POST-IMPLANTATION DUE TO STIFFNESS AND DECREASED RANGE OF MOTION. THE FEMORAL AND TIBIAL INSERT WERE REMOVED AND REPLACED.

  Patient problems: Loss of Range of Motion

  MAUDE report 19336613 ↗
• InjuryMay 2, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Insufficient Information

  MAUDE report 19234565 ↗
• InjurySep 22, 2022Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THE PATIENT UNDERWENT A RIGHT KNEE MANIPULATION UNDER ANESTHESIA APPROXIMATELY FORTY DAYS POST-IMPLANTATION DUE TO SCAR TISSUE, PAIN, STIFFNESS, AND LIMITED FLEXION. IT WAS REPORTED RESOLVED THE SAME DAY AND ALL IMPLANTS REMAIN IN PLACE.

  Patient problems: Loss of Range of Motion; Pain; Scar Tissue

  MAUDE report 15465034 ↗
• InjuryMay 20, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL TOTAL KNEE ARTHROPLASTY. SUBSEQUENTLY, THE IMPLANTED ARTICULAR SURFACE DISLOCATED POSTOPERATIVELY AND THE PATIENT UNDERWENT A REVISION PROCEDURE TO REPLACE THE DISLOCATED IMPLANT APPROXIMATELY 23 DAYS LATER. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Joint Dislocation

  MAUDE report 14455378 ↗