BULLSEYE C8660Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854034293), received between Sep 9, 2025 and Sep 9, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Fragmentation” (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.

• MalfunctionSep 9, 2025Material Fragmentation; Material Fragmentation

  THE CUSTOMER REPORTED THAT THE DEVICE, C8660, BULLSEYE FEMORAL GUIDE, 8 MM/9 MM, WAS BEING USED DURING AN UNKNOWN PROCEDURE ON (B)(6) 2025 WHEN IT WAS REPORTED, ¿IT WAS REPORTED BY SURGICAL TECHNOLOGIST THAT THE GUIDE BROKE INSIDE THE PATIENT DURING THE PROCEDURE. NO FRAGMENTS REMAINED INSIDE THE PATIENT; THE SURGEON WAS ABLE TO REMOVE THE PIECE THAT WAS IN THE PATIENT'S KNEE.¿. THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, OR HOSPITALIZATION OF THE PATIENT. CONMED WAS ADVISED NO FURTHER INFORMATION IS KNOWN. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23007283 ↗