BEUDAMED
    FDA Adverse Event Other Summary report: N

    CONMED

    MDR report key: 416849 · Received September 17, 2002

    Report

    Report Number
    416849
    Event Type
    Other
    Date Received
    September 17, 2002
    Date of Event
    August 19, 2002
    Report Date
    September 12, 2002
    Manufacturer
    CONMED
    Product Code
    GEI
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DR STATES SUSTAINED A SMALL 2ND DEGREE BURN ON THEIR RIGHT FOREARM FROM TOUCHING THE CLAMP THAT WAS HOLDING A CONTAINER THAT HOUSED THE BOVIE DURING A C/SECTION. THE MD FELT A "ZING", BUT SAW NO SPARK. THE PT WAS GROUNDED DURING SURGERY. FOLLOWING SURGERY, DR WAS TREATED IN THE ED FOR THE 2ND DEGREE BURN. PT RECEIVED A TETANUS SHOT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CONMED ELECTRIC SURGICAL GENERATOR GEI CONMED SABRE 2400 *

    Patients

    Seq Age Sex Outcome Treatment
    1 41 YR Other ACTIVE PENCIL & RETURN PAD. RETURNED ALSO FOR| EVALUATION.