BEUDAMED
    FDA Adverse Event Injury Summary report: N

    JUNI

    MDR report key: 2981523 · Received February 27, 2013

    Report

    Report Number
    1020279-2013-00133
    Event Type
    Injury
    Date Received
    February 27, 2013
    Date of Event
    June 5, 2009
    Report Date
    February 25, 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 THE SURGEON PERFORMED MANIPULATION UNDER ANETHESIA DUE TO STIFFNESS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    83842 JUNI JOURNEY UNI TIB BASE RM/LL SZ 4 JWH SMITH & NEPHEW, INC. 08LM17765

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Required Intervention