BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OCL

    MDR report key: 250756 · Received November 17, 1999

    Report

    Report Number
    1928508-1999-00002
    Event Type
    Injury
    Date Received
    November 17, 1999
    Date of Event
    June 22, 1997
    Report Date
    November 16, 1999
    Manufacturer
    M-PACT WORLD WIDE MANAGEMENT
    Product Code
    FYH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    CELLULITIS OR BURN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OCL SPLINT FYH M-PACT WORLD WIDE MANAGEMENT NR NR

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR Hospitalization