BEUDAMED
    FDA Adverse Event Other Summary report: N

    KARL STORZ

    MDR report key: 1080689 · Received July 1, 2008

    Report

    Report Number
    2020550-2008-00014
    Event Type
    Other
    Date Received
    July 1, 2008
    Date of Event
    May 30, 2008
    Report Date
    June 30, 2008
    Manufacturer
    D & R PRODUCTS CO.
    Product Code
    GFF
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    DOCTOR WAS PERFORMING A RIGHT SHOULDER ARTHROSCOPY; ALLEGEDLY, AFTER THE PROCEDURE, IT WAS NOTED THAT PT HAD RECEIVED A 1'X7MM SUPERFICIAL BURN ON SHOULDER. OTHER THAN LOOSE BANDAGE, NO MEDICAL ATTENTION WAS NECESSARY. PROCEDURE WAS COMPLETED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KARL STORZ DISPOSABLE BURR GFF D & R PRODUCTS CO. 28205HDS 23980

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other