Persona® 42-5399-051-95Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889024582842), received between May 26, 2022 and Sep 30, 2022 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Mechanical Jam” (3 reports).

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.

• MalfunctionSep 30, 2022Mechanical Jam; Mechanical Jam

  THE WAREHOUSE RECEIVED A CUTTING BLOCK WITH A PIN STUCK IN A HOLE. THE PIN IS BROKEN. ITEMS WERE IN A LOANER SET. NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15511987 ↗
• MalfunctionJul 28, 2022Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT DURING A PARTIAL KNEE ARTHROPLASTY, THE DRILL PIN BECAME JAMMED IN THE TIBIAL CUT GUIDE. THE PROCEDURE WAS COMPLETED UTILIZING ANOTHER DEVICE. NO ADVERSE EVENTS WERE REPORTED AS A RESULT OF THIS MALFUNCTION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15121589 ↗
• MalfunctionMay 26, 2022Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT DURING A PARTIAL KNEE ARTHROPLASTY, THE DRILL PIN BECAME JAMMED IN THE TIBIAL CUT GUIDE. THE PROCEDURE WAS COMPLETED UTILIZING ANOTHER DEVICE. NO ADVERSE EVENTS WERE REPORTED AS A RESULT OF THIS MALFUNCTION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14516823 ↗