BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SOUTHMEDIC #20 STERILE BLADE

    MDR report key: 6945563 · Received October 2, 2017

    Report

    Report Number
    6945563
    Event Type
    Injury
    Date Received
    October 2, 2017
    Date of Event
    September 13, 2017
    Report Date
    September 15, 2017
    Manufacturer
    SOUTHMEDIC INC.
    Product Code
    GES
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    AL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    A SOUTHMEDIC #20 BLADE RIPPED THE PT'S SKIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    688970 SOUTHMEDIC #20 STERILE BLADE #20 STERILE BLADE GES SOUTHMEDIC INC. 34165

    Patients

    Seq Age Sex Outcome Treatment
    1 60 YR