HAND-TROL GOLD LINE 60-0300-501Recalls & reported problems
Conmed Corporation · HAND-TROL GOLD LINE, ELECTROSURGICAL HANDPIECE · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30653405008266), received between Jun 30, 2016 and Jun 30, 2016 — classified as 1 injury.
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 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Burn(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 30, 2016Adverse Event Without Identified Device or Use Problem
A (B)(6) WITH OSA AND ADENOTONSILLAR HYPERTROPHY TAKEN TO OPERATING ROOM FOR A TONSILLECTOMY AND ADENOIDECTOMY. INCISION MADE TO REMOVE THE TONSILS USING AN ELECTRO CAUTERY UNIT. AFTER THE REMOVAL OF THE TONSILS, BURNS WERE NOTED OF THE ORAL COMMISSURE. THE BURN ON THE RIGHT WAS VERY SUPERFICIAL. THE BURN ON THE LEFT WAS MORE SIGNIFICANT. THE SURGEON BELIEVES THERE WAS A LEAK OF CURRENT FROM THE BOVIE HANDLE THAT CAUSED THE BURN.
Patient problems: Burn(s)
MAUDE report 5771836 ↗
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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