CONMED GOLDLINE 130318ARecalls & reported problems
Conmed Corporation · CONMED GOLDLINE ELECTROSURGICAL HANDPIECE, HAND CONTROLLED WITH BLADE ELECTRODE, BUTTON SWITCH, SAFETY HOLSTER AND 10' (3 M) CABLE · Class 2
All models of CONMED GOLDLINE (10)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20653405056307), received between Jul 7, 2025 and Jul 7, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Superficial (First Degree) Burn1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 7, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
A DISTRIBUTOR REPORTED ON BEHALF OF A CUSTOMER THAT THE 130318A, ELECTROSURGICAL HANDPIECE DEVICE WAS USED IN AN UNNAMED PROCEDURE ON (B)(6) 2025, AND ¿DURING SURGERY THE CAUTERY THE PROVIDER WAS USING CAUSED A SMALL (FIRST DEGREE) BURN TO THE SIDE OF THE PATIENT'S MOUTH¿. THROUGH FURTHER ASSESSMENT, THE DISTRIBUTOR INDICATED THE EVENT WAS ALSO REPORTED TO THE FDA BY THE CUSTOMER UNDER REPORT NUMBER MW5171051, AND "THE CUSTOMER HAS NOT RESPONDED AFTER MULTIPLE ATTEMPTS TO GET MORE INFORMATION.". THIS REPORT IS BEING RAISED ON THE BASIS OF MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: Superficial (First Degree) Burn
MAUDE report 22422218 ↗
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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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