BEUDAMED
    FDA Adverse Event Injury Summary report: N

    KARL STORZ

    MDR report key: 19385 · Received September 16, 1994

    Report

    Report Number
    2020550-1994-00038
    Event Type
    Injury
    Date Received
    September 16, 1994
    Date of Event
    June 14, 1994
    Report Date
    September 8, 1994
    Manufacturer
    KAARL STORZ GMBH & CO.
    Product Code
    FFZ
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    SC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CAUTERY UNIT WAS NOT ACTIVATED, BUT THE SCISSORS WERE ENERGIZED VIA A KARL STORZ H.F. CABLE AND BURNED THE PT'S COLON.BOWEL WEDGE RESECTION WAS PERFORMED WITH LOW TRANSVERSE INCISION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KARL STORZ H.F. CORD FFZ KAARL STORZ GMBH & CO. 26000M

    Patients

    Seq Age Sex Outcome Treatment
    1 * Hospitalization| R