Persona® 42-5726-064-02Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024576186), received between Feb 17, 2023 and Sep 2, 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.

• InjurySep 2, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL RIGHT TOTAL KNEE ARTHROPLASTY COMPLETED. APPROXIMATELY 3 MONTHS POST-OP, THE PATIENT EXPERIENCED STIFFNESS AND LIMITED RANGE OF MOTION. SUBSEQUENTLY, THE PATIENT UNDERWENT A MANIPULATION UNDER ANESTHESIA AND THE PATIENT'S SYMPTOMS HAVE REPORTEDLY IMPROVED. ATTEMPTS HAVE BEEN MADE AND ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.

  Patient problems: Arthrofibrosis; Loss of Range of Motion

  MAUDE report 22936296 ↗
• InjuryFeb 17, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE INITIAL RIGHT TOTAL KNEE ARTHROPLASTY WAS PERFORMED. SUBSEQUENTLY, THE PATIENT UNDERWENT A MANIPULATION UNDER ANESTHESIA DUE TO STIFFNESS AND LIMITED RANGE OF MOTION APPROXIMATELY 2 MONTHS POST PROCEDURE. AUDIBLE ADHESIONS WERE RELEASED, AND AN INTRAOP RANGE OF MOTION OF 0-135 DEGREES WAS ACHIEVED.

  Patient problems: Adhesion(s); Loss of Range of Motion

  MAUDE report 16396600 ↗