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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 1 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

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 ↗

Other BATTERY, REPLACEMENT, RECHARGEABLE devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.