CONMED PRO3520Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854012918), received between Jan 4, 2018 and Jan 4, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Connection Problem” (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.

• InjuryJan 4, 2018Connection Problem; Connection Problem

  THE DISTRIBUTOR REPORTED A BATTERY EXPLODED IN THEIR SALES REPRESENTATIVES HAND IN TURKEY. THIS "EXPLOSION" WAS REPORTED TO HAVE CAUSED THE SALES REPRESENTATIVE TO LOOSE VISION FOR APPROXIMATELY 20-25 MINUTES. HIS HAND WAS NOT BURNED NOR WAS A PHYSICAL SHOCK DELIVERED FROM THE DEVICE. THIS "EXPLOSION" TOOK PLACE IN THE SUPPLY ROOM WHEN THE SALES REPRESENTATIVE REMOVED THE BATTERY FROM THE CHARGE PLATFORM TO BRING IT INTO THE OR. THIS REPORT IS RAISED ON THE BASIS OF A REPORTED INJURY.

  Patient problems: Blurred Vision

  MAUDE report 7163470 ↗