MERLIN C9241Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854012512), received between Jul 15, 2019 and Jul 15, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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 16, 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.

• MalfunctionJul 15, 2019Break; Break

  THE CONMED REPRESENTATIVE REPORTED ON BEHALF OF THE FACILITY THAT THE C9241, 4.2MM MERLIN BUR'S TIP BECAME DISENGAGED FROM THE INNER HUB DURING USE IN A KNEE ARTHROSCOPY ON (B)(6) 2019. THERE WAS NO PATIENT OR USER INJURY. THE PROCEDURE WAS COMPLETED. THIS REPORT IS BEING RAISED BASED ON DEVICE MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8788868 ↗