BEUDAMED
    FDA Adverse Event Summary report: N

    *

    MDR report key: 3586871 · Received January 16, 2014

    Report

    Report Number
    3586871
    Date Received
    January 16, 2014
    Date of Event
    January 10, 2014
    Report Date
    January 16, 2014
    Manufacturer
    CAREFUSION 213 LLC
    Product Code
    LWK
    Report Source
    User Facility report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PATIENT SHAVED PRE-OPERATION WITH SURGICAL CLIPPER USING THE NEURO BLADE. SKIN ABRASIONS NOTED TO LEFT LOWER QUADRANT OF ABDOMEN FOLLOWING THE UNDRAPING OF THE PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    41902 * CLIPPER LWK CAREFUSION 213 LLC 4412A *

    Patients

    Seq Age Sex Outcome Treatment
    1 45 YR