BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1043534-2012-00476

    MDR report key: 2858614 · Received December 5, 2012

    Report

    Report Number
    1043534-2012-00476
    Event Type
    Malfunction
    Date Received
    December 5, 2012
    Report Date
    April 30, 2012
    Manufacturer
    WRIGHT MEDICAL TECHNOLOGY, INC.
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    OTHER
    Health Professional
    N

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown