Persona® 42-5726-060-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889024576063), received between Jul 8, 2021 and Dec 9, 2025 — classified as 2 injuries, 1 malfunction.

The most frequently reported specific device problem is “Material Erosion” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryDec 9, 2025Material Erosion; Material Erosion

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

  Patient problems: Metal Related Pathology

  MAUDE report 23760622 ↗
• MalfunctionJun 14, 2022Use of Device Problem; Use of Device Problem

  IT WAS REPORTED THAT INCORRECT PRODUCT WAS IMPLANTED INTO A PATIENT. THE SURGEON AND THE SALES REPRESENTATIVE THAT WAS IN THE ROOM WERE FOLLOWED UP WITH TO MAKE THEM AWARE OF THE ISSUE. I WAS INFORMED THAT THE REGULAR PROCESS OF CHECKING THE IMPLANT WITH THE HOSPITAL STAFF DID OCCUR BEFORE THE IMPLANT WAS OPENED, HOWEVER AT THE TIME, NO ONE RECOGNIZED THE ISSUE. THERE IS NO ADDITIONAL INFORMATION AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14686774 ↗
• InjuryJul 8, 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 5 AND A HALF MONTHS¿ POST IMPLANTATION DUE TO SEVERE PAIN AND ARTHROFIBROSIS. DESPITE CORTISONE INJECTIONS AND MANIPULATION, THE PATIENT CONTINUED TO HAVE MODERATE/SEVERE PAIN AND PROBLEMS AT THE ONE YEAR FOLLOW UP VISIT. NO FURTHER INTERVENTION HAS BEEN PLANNED TO DATE. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE INFORMATION IS AVAILABLE.

  Patient problems: Ambulation or Postural Difficulties; Loss of Range of Motion; Pain; Scar Tissue; Swelling/ Edema

  MAUDE report 12135914 ↗