Bovie IDS-310Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10607151008946), received between Oct 29, 2019 and Oct 29, 2019 — classified as 1 malfunction.

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

• MalfunctionOct 29, 2019Fire; Sparking

  AN IDS-310 UNIT IS GENERATING A SPARK THAT IS NOT NORMAL. IT HAD TO BE WITHDRAWN FROM THE SURGERY ROOM AS SINCE THERE WAS FIRE IN SURGERY ROOM, RESULTING IN A BURN TO THE PATIENT. THE FIRE WAS CAUSED BY A SPARK THAT CAME INTO CONTACT WITH THE OXYGEN.

  Patient problems: Burn, Thermal

  MAUDE report 9249898 ↗