BEUDAMED
    FDA Adverse Event Injury Summary report: N

    K-WIRE

    MDR report key: 483878 · Received September 17, 2003

    Report

    Report Number
    9616696-2003-00005
    Event Type
    Injury
    Date Received
    September 17, 2003
    Report Date
    August 14, 2003
    Manufacturer
    STRYKER INSTRUMENTS
    Product Code
    DZK
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    INFECTION AT K WIRE SITES WERE DOCUMENTED BY THE DOCTOR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 K-WIRE WIRE, FIXATION, INTRAOSSEOUS DZK STRYKER INSTRUMENTS 5300-006-035 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention