BEUDAMED
    FDA Adverse Event Summary report: N

    *

    MDR report key: 2181716 · Received July 13, 2011

    Report

    Report Number
    2181716
    Date Received
    July 13, 2011
    Date of Event
    May 6, 2011
    Report Date
    July 13, 2011
    Manufacturer
    MEDLINE
    Product Code
    LWK
    Report Source
    User Facility report
    Reporter Location
    MD, US

    Narratives

    Description of Event or Problem · 1

    THERE ARE FOUR WRITTEN REPORTS AND SEVERAL VERBAL REPORTS THAT INDICATE WHEN USING CLIPPERS PRIOR TO PROCEDURES, ABRASIONS, SCRATCHES, AND NICKS WERE FOUND ON THE PATIENT AFTER USE OF THE CLIPPER. THIS PRODUCT HAS BEEN USED AT THIS FACILITY FOR APPROXIMATELY THREE YEARS. THIS ISSUE JUST STARTED TO OCCUR IN THE SPRING OF THIS YEAR ACCORDING TO MY KNOWLEDGE. THERE IS NO LARGE TURNOVER OF STAFF.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * SURGICAL, RAZOR LWK MEDLINE * *

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR OTHER
    2 60 YR
    3 40 YR
    4 59 YR