Skip to content

Persona® 42-5706-058-01Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

All models of PERSONA (364)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024576476), received between Feb 8, 2023 and Feb 8, 2023 — classified as 1 injury.

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

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Loss of Range of Motion1
  • Scar Tissue1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryFeb 8, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED VIA A CLINICAL STUDY THAT A PATIENT UNDERWENT AN INITIAL LEFT TOTAL KNEE ARTHROPLASTY. SUBSEQUENTLY, APPROXIMATELY TWO MONTHS POST-IMPLANTATION, THE PATIENT EXPERIENCED LIMITED RANGE OF MOTION DUE TO FIBROSIS AND UNDERWENT A MANIPULATION UNDER ANESTHESIA PROCEDURE. THE PROCEDURE WAS COMPLETED WITHOUT COMPLICATION.

    Patient problems: Loss of Range of Motion; Scar Tissue

    MAUDE report 16327000 ↗

Other Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive devices

All Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page