Persona® 42-5700-058-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024576278), received between Feb 24, 2022 and May 7, 2025 — classified as 2 injuries.

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

• InjuryMay 7, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE CLINICAL STUDY PATIENT EXPERIENCED PAIN IN THE BACK OF LEFT KNEE APPROXIMATELY ON YEAR, NINE MONTHS POST IMPLANTATION AND WAS PRESCRIBED PHYSICAL THERAPY. REPORTED IMPROVING, AND REMAINS IMPLANTED. THERE IS NO ADDITIONAL INFORMATION.

  Patient problems: Pain

  MAUDE report 21980542 ↗
• InjuryFeb 24, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED PATIENT MANIPULATION UNDER ANESTHESIA DUE TO STIFFNESS AND LIMITED RANGE OF MOTION IN KNEE TWO MONTHS POST IMPLANTATION. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE IS AVAILABLE.

  Patient problems: Loss of Range of Motion

  MAUDE report 13592982 ↗