Persona® Trabecular Metal® 42-5022-068-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889024470132), received between Sep 27, 2024 and Apr 9, 2026 — classified as 2 injuries, 1 malfunction.

The most frequently reported specific device problem is “Device Damaged Prior to Receipt by User” (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.

• MalfunctionApr 9, 2026Device Damaged Prior to Receipt by User

  IT WAS REPORTED THE IMPLANT PACKAGING APPEARED TO BE DAMAGED PRIOR TO USE. THE DEVICE WAS NOT USED AND NO PATIENT IMPACT AND NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION. ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24835076 ↗
• InjuryOct 9, 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: Erosion; Pain

  MAUDE report 20407684 ↗
• InjurySep 27, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A LEFT KNEE MANIPULATION UNDER ANESTHESIA TO ADDRESS KNEE STIFFNESS AND LIMITED RANGE OF MOTION APPROXIMATELY SEVEN (7) WEEKS FOLLOWING LEFT KNEE ARTHROPLASTY. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED. INITIAL OPERATIVE NOTES NOTED NO INTRAOPERATIVE COMPLICATIONS. MANIPULATION OPERATIVE NOTES NOTED THE PATIENT'S RANGE OF MOTION WAS 85 DEGREES PREOPERATIVELY. MANIPULATION WAS PERFORMED SUCCESSFULLY AND THE PATIENT'S RANGE OF MOTION WAS 125 DEGREES AT THE CONCLUSION OF THE PROCEDURE. NO INTRAOPERATIVE COMPLICATIONS WERE NOTED.

  Patient problems: Loss of Range of Motion; Scar Tissue

  MAUDE report 20320344 ↗