SYSTEM 2450 60-2450-230Recalls & reported problems
Conmed Corporation · SYSTEM 2450 230 - 240 VAC 50/60 Hz Electrosurgical Unit · Class 2
Data updated Oct 16, 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 20653405058165), received between Jun 23, 2025 and Jun 23, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unintended Electrical Shock” (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.
Reports received per month
Most reported problems
Device problems
- Unintended Electrical Shock1
Patient problems
- Electric Shock1
- Shock1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 23, 2025Unintended Electrical Shock; Unintended Electrical Shock
THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE 60-2450-230 SYSTEM 2450 230 - 240 VAC 50/60 HZ ELECTROSURGICAL UNIT WAS BEING USED ON (B)(6)2025 AND ¿THE OPERATOR HAS RECEIVED AN ELECTRIC SHOCK TO HIS FINGER¿. THERE WAS NO IMPACT OR INJURY FOR THE PATIENT OR USER. THE PROCEDURE WAS COMPLETED WITH AN ALTERNATE DEVICE. A GOOD FAITH EFFORT HAS BEEN COMPLETED; HOWEVER, TO DATE NO NEW INFORMATION HAS BEEN RECEIVED. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: Electric Shock; Shock
MAUDE report 22308473 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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