THERMOGARD 51-7810Recalls & reported problems
Conmed Corporation · THERMOGARD DUAL DISPERSIVE ELECTRODE · 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 10653405007494), received between Feb 6, 2018 and Feb 6, 2018 — classified as 1 injury.
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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Insufficient Device Problem Information1
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.
InjuryFeb 6, 2018Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information
THE USER FACILITY REPORTED THAT DURING A LOOP ELECTROSURGICAL EXCISION PROCEDURE, THE 51-7810 THERMOGARD BURNED THE PATIENT'S LEFT THIGH. THE INJURY WAS FOUND POST-OPERATIVELY AND DESCRIBED AS "IT HAD BLISTERS AND WAS WHITE AND HARD." THE PATIENT WAS TREATED WITH SILVADENE CREAM AND COVERED WITH TELSA NON-ADHERING DRESSING. THE PROCEDURE WAS COMPLETED WITH NO OTHER INCIDENTS OR SURGICAL DELAYS. UPON GATHERING ADDITIONAL INFORMATION, THE PATIENT WAS DISCHARGED HOME WITH NO ADDITIONAL HOSPITAL STAY DUE TO THIS INCIDENT. THIS REPORT IS RAISED BASED ON A REPORTED PATIENT INJURY.
Patient problems: Burn(s)
MAUDE report 7243783 ↗
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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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