Persona® Trabecular Metal® 42-5022-062-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00889024470071), received between Mar 16, 2021 and Feb 2, 2026 — classified as 5 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 2, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL LEFT KNEE SURGERY. APPROXIMATELY 3.5 YEARS POSTOP, THE PATIENT WAS REVISED DUE TO PAIN. ATTEMPTS HAVE BEEN MADE AND ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.

  Patient problems: Pain

  MAUDE report 24232897 ↗
• InjuryApr 28, 2025Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth

  IT WAS REPORTED THAT A PATIENT UNDERWENT AN INITIAL LEFT KNEE ARTHROPLASTY. APPROXIMATELY 2 MONTHS POST-OPERATION, THE PATIENT WAS REVISED DUE TO FEMORAL LOOSENING AND PAIN. ATTEMPTS HAVE BEEN MADE AND ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.

  Patient problems: Aseptic loosening; Pain

  MAUDE report 21918519 ↗
• InjurySep 22, 2022Insufficient Device Problem Information; Insufficient Device Problem Information

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

  Patient problems: Loss of Range of Motion; Scar Tissue

  MAUDE report 15465158 ↗
• InjuryApr 19, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT UNDERWENT LEFT TOTAL KNEE ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT UNDERWENT A MANIPULATION UNDER ANESTHESIA DUE TO ARTHROFIBROSIS APPROXIMATELY 2 MONTHS LATER. THE ISSUE RESOLVED, AND THE PATIENT HAD FULL RANGE OF MOTION WITH NO COMPLAINTS AT THE NEXT FOLLOW UP VISIT. NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Loss of Range of Motion; Scar Tissue

  MAUDE report 11685893 ↗
• InjuryMar 16, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT A MANIPULATION UNDER ANESTHESIA APPROXIMATELY TWO MONTHS AND ONE-WEEK POST IMPLANTATION DUE TO ARTHROFIBROSIS. THE PATIENT COMPLETED THE STUDY SATISFIED APPROXIMATELY ONE YEAR AND FIVE MONTHS LATER WITHOUT FURTHER COMPLICATIONS REQUIRING INTERVENTION. THERE IS NO ADDITIONAL INFORMATION AT THIS TIME.

  Patient problems: Loss of Range of Motion; Scar Tissue

  MAUDE report 11495841 ↗