BEUDAMED
    FDA Adverse Event Injury Summary report: N

    JET-X

    MDR report key: 1051719 · Received May 23, 2008

    Report

    Report Number
    1020279-2008-00157
    Event Type
    Injury
    Date Received
    May 23, 2008
    Report Date
    May 12, 2008
    Manufacturer
    SMITH & NEPHEW, INC., OTHOPAEDIC DIV.
    Product Code
    HTY
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    NA

    Description of Event or Problem · 1

    THE PT UNDERWENT REVISION SURGERY DUE TO THE CLAMP DISASSEMBLING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 JET-X EXTERNAL FIXATION HTY SMITH & NEPHEW, INC., OTHOPAEDIC DIV. 07GM18395

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Other