BEUDAMED
    FDA Adverse Event Other Summary report: N

    LIQUID LIGHT CABLE

    MDR report key: 103008 · Received June 19, 1997

    Report

    Report Number
    1216828-1997-00003
    Event Type
    Other
    Date Received
    June 19, 1997
    Date of Event
    June 13, 1997
    Report Date
    June 19, 1997
    Manufacturer
    SMITH & NEPHEW, INC ENDOSCOPY DIVISION
    Product Code
    FSW
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    CO, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    THE SURGEON LAYED THE RIGHT CABLE ON THE PT. THERE WERE NO BURNS ON THE DRAPES, HOWEVER, A "SLASH" BURN WAS OBSERVED ON THE PT'S ABDOMEN WHEN THE DRAPES WERE REMOVED. SIZE AND DEGREE OF THE BURN WAS NOT KNOWN BY THE HOSPITAL CONTACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIQUID LIGHT CABLE LIGHT CABLE FSW SMITH & NEPHEW, INC ENDOSCOPY DIVISION NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 27 YR Other