Persona® PPS® 42-5086-070-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889024631373), received between Jul 24, 2024 and Jan 20, 2026 — classified as 2 injuries, 1 malfunction.

The most frequently reported specific device problem is “Use of Device Problem” (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.

• InjuryJan 20, 2026Adverse Event Without Identified Device or Use Problem

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

  Patient problems: Joint Laxity; Loss of Range of Motion; Pain

  MAUDE report 24120953 ↗
• InjuryJul 24, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

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

  Patient problems: Fluid Discharge; Impaired Healing

  MAUDE report 19817316 ↗
• MalfunctionJul 24, 2024Use of Device Problem; Use of Device Problem

  IT WAS REPORTED THAT THE WRONG PRODUCT WAS IMPLANTED INTO A PATIENT. THE PATIENT ACCIDENTALLY RECEIVED CEMENTLESS IMPLANTS INTRAOPERATIVELY. THERE IS NO ADDITIONAL INFORMATION AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19817210 ↗