BEUDAMED
    FDA Adverse Event Other Summary report: N

    AESCULAP CABLE

    MDR report key: 435843 · Received January 3, 2003

    Report

    Report Number
    435843
    Event Type
    Other
    Date Received
    January 3, 2003
    Date of Event
    September 24, 2002
    Report Date
    October 18, 2002
    Manufacturer
    AESCULAP, INC
    Product Code
    GEI
    Report Source
    User Facility report
    Reporter Location
    MD, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    CAUTERY CORD SHORT. DURING A SURGICAL PROCEDURE THE CAUTERY CORD CAUGHT FIRE. FACTORS THAT MIGHT PREVENT FUTURE OCCURRENCES: APPROPRIATE TRAINING, BETTER DEVICE MAINTENANCE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AESCULAP CABLE REUSABLE MONOPOLAR CABLE GEI AESCULAP, INC UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 41 YR Other