BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1020279-2013-00051

    MDR report key: 2934622 · Received January 30, 2013

    Report

    Report Number
    1020279-2013-00051
    Event Type
    Injury
    Date Received
    January 30, 2013
    Report Date
    January 23, 2013
    Manufacturer
    SMITH & NEPHEW, INC.
    Product Code
    JWH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A ARTHROSCOPIC EVALUATION WAS PERFORMED DUE TO PAIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    41305 JWH SMITH & NEPHEW, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention