Persona® 42-5870-002-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024558861), received between Mar 29, 2022 and Mar 29, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical Jam” (1 report).

1 other recall cover devices cleared under the same FDA submission (K181947, K191625); they may or may not involve this specific model.

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

• MalfunctionMar 29, 2022Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT DURING A LEFT KNEE PROCEDURE, A DRILL PIN COLD WELDED TO THE RESECTION GUIDE. THE DRILL PIN LATER FRACTURED WHEN ATTEMPTING TO REMOVE IT FROM THE GUIDE AFTER SURGERY. THERE WAS NO SURGICAL DELAY OR PATIENT IMPACT AND THE PROCEDURE WAS ABLE TO PROCEED WITHOUT FURTHER INCIDENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN MADE AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13938025 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K181947, K191625. One submission often covers many models, so check the product and lot details in each record.

• Z-2578-2026 · May 11, 2026 · Open, Classified
  Brand Name: Persona Revision Product Name: Persona Revision Trabecular Metal Femoral Distal Augment Model/Catalog Number: 42-5572-066-10 Software Version: N/A Product Description: