Persona® Trabecular Metal® 42-5022-066-02Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024470125), received between Jul 10, 2023 and Feb 9, 2026 — classified as 4 injuries.

The most frequently reported specific device problem is “Inadequacy of Device Shape and/or Size” (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.

• InjuryFeb 9, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A RIGHT KNEE ARTHROPLASTY REVISION TO ADDRESS INSTABILITY APPROXIMATELY ONE (1) MONTH POST-OPERATIVELY. ATTEMPTS HAVE BEEN MADE, HOWEVER, NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: Joint Laxity

  MAUDE report 24293746 ↗
• InjuryJul 11, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THROUGH A JOURNAL ARTICLE AND STUDY THAT ONE PATIENT UNDERWENT MANIPULATION UNDER ANESTHESIA DUE TO LIMITED RANGE OF MOTION APPROXIMATELY 6 WEEKS POST IMPLANTATION. ATTEMPTS FOR ADDITIONAL INFORMATION ARE IN PROGRESS AND NONE HAS BEEN PROVIDED.

  Patient problems: Loss of Range of Motion

  MAUDE report 22480652 ↗
• InjuryApr 24, 2024Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size

  IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL SURGERY. APPROXIMATELY ONE YEAR LATER, THE PATIENT WAS REVISED DUE TO LOOSENING, PAIN, AND INSTABILITY. DURING THE SURGERY, THE SURGEON ALSO NOTED THAT THE FEMORAL COMPONENT WAS INTERNALLY ROTATED AND OVERSIZED. ONLY THE TIBIAL COMPONENT AND POLY WERE REVISED. ATTEMPTS HAVE BEEN MADE AND ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.

  Patient problems: Joint Laxity; Pain

  MAUDE report 19172679 ↗
• InjuryJul 10, 2023Malposition of Device; Malposition of Device

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

  Patient problems: Failure of Implant; Pain

  MAUDE report 17292254 ↗