CONMED L3000Recalls & reported problems
Conmed Corporation · Lithium Battery Charger · Class 1
- 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 10845854041369), received between Apr 1, 2024 and Apr 1, 2024 — 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Unintended Electrical Shock1
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.
MalfunctionApr 1, 2024Unintended Electrical Shock; Unintended Electrical Shock
THE CUSTOMER REPORTED THAT L3000, LITHIUM BATTERY CHARGER, WAS BEING USED DURING A NON-SURGICAL EVENT ON (B)(6) 2024 WHEN IT WAS REPORTED ¿ONE OF THE CENTRAL STERILIZATION EMPLOYEES RECEIVED AN ELECTRIC SHOCK ON A FINGER RESULTING IN MINOR INJURIES: 'ENTRANCE' AND 'EXIT' BURNS ON THE FINGER. THIS OCCURRED WHILE SLIDING A BATTERY INTO/OUT OF THE CONMED L3000 BATTERY CHARGER WITH SERIAL NUMBER (B)(6) THAT WE RECEIVED FROM YOU AS A LOANER TO TEMPORARILY REPLACE OUR DEFECTIVE BATTERY CHARGER. THE EMPLOYEE PUSHED THE BATTERY INTO THE BATTERY CHARGER, BUT IT DID NOT START CHARGING (THE DISPLAY DID NOT LIGHT UP). SO SHE PUSHED THE BATTERY OUT OF THE BATTERY CHARGER AGAIN, AT WHICH POINT SHE RECEIVED A POWER SHOCK.¿. IT WAS ALSO REPORTED THAT THE USER WAS NOT WEARING ANY JEWELRY, AND NOTHING WAS OUT OF ORDINARY WITH THE DEVICE. FURTHER ASSESSMENT QUESTIONING FOUND THAT THE USER WAS DIAGNOSED WITH A 1ST DEGREE BURN AND WAS TREATED WITH ¿WOUND CARE OF A FIRST-DEGREE BURN. THE ACCIDENT WITH THE BATTERY CHARGER HAPPENED AT THE STERILIZATION DEPARTMENT. BEFORE STERILIZING THE BATTERY, THE EMPLOYEE CONCERNED WILL TEST THE STATE OF CHARGE OF THE BATTERY. TO DO THIS, SHE SLIDES THE BATTERY IN AND
Patient problems: Superficial (First Degree) Burn
MAUDE report 19012380 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.