CONMED 00502318300Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854003978), received between Aug 31, 2026 and Aug 31, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Expiration Date Error” (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 31, 2026Expiration Date Error

  The distributor reported on behalf of their customer that the device, 00502318300, ACL BLADE, FINE, 9.5 X 25.5 X 0.4 MM, was used during a bone cement procedure on (b)(6) 2026 when it was reported, ¿It was reported that after the procedure, it was found that the saw blade used during the procedure was expired.¿ There was no report of medical intervention or hospitalization for the patient. The procedure was completed as planned. Further assessment from the reporter found, ¿I hereby report that, to date, I have received no reports regarding any issues with the patient in question; according to information received from the surgical support, the surgery concluded without incident.¿ There were no allegations that the labeling was incorrect on the device.This report is being raised due to the reported injury of expired device used on patient.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50518312 ↗