CONMED PRO6240Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854018934), received between Jun 3, 2024 and Jun 3, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Excessive Heating” (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. How this data works · Data updated Oct 13, 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.

• MalfunctionJun 3, 2024Excessive Heating; Excessive Heating

  THE CUSTOMER REPORTED THAT THE PRO6240, 1.8-4MM PIN DRIVER, DEVICE WAS BEING USED DURING AN UNKNOWN PROCEDURE ON (B)(6) 2024 WHEN IT WAS REPORTED ¿THE PATIENT'S SKIN HAS BEEN BURNED.¿. FURTHER ASSESSMENT QUESTIONING FOUND THAT THE PATIENT DID RECEIVE A SMALL BURN, BUT THE DEGREE IS UNKNOWN. THEY PUT ON A BANDAGE, & THE SURGEON DIDN¿T RECEIVE ANY COMPLAINTS FROM THE CONSIGNEE. THE PROCEDURE WAS COMPLETED WITH AN UNKNOWN ALTERNATE DEVICE. THERE WAS NO REPORT OF MEDICAL INTERVENTION, OR EXTENDED HOSPITALIZATION FOR THE PATIENT OR USER. THIS REPORT IS BEING RAISED ON THE BASIS OF MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: Burn(s)

  MAUDE report 19446245 ↗