CONMED C8623Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854034255), received between Aug 26, 2026 and Aug 26, 2026 — classified as 1 injury.

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.

• InjuryAug 26, 2026Material Fragmentation

  A distributor reported on behalf of a customer that the device, C8623, TWO PIN PASSER DRILL TIP, 15.5", was used in an ACL procedure on (b)(6) 2026, and ¿during the surgery, this complaint product was fractured during use, and the fractured piece of it has remained inside of the patient¿s body.¿ The procedure was completed with a delay of about 30 minutes. There was no report of medical/surgical intervention, or extended hospitalization for the patient. This report is being raised due to the reported injury of a foreign body retained in the patient.

  Patient problems: Foreign Body In Patient

  MAUDE report 50451288 ↗