BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CONSERVE(R) PLUS HA CUP

    MDR report key: 3241571 · Received July 22, 2013

    Report

    Report Number
    1043534-2013-01179
    Event Type
    Injury
    Date Received
    July 22, 2013
    Date of Event
    May 7, 2013
    Report Date
    June 18, 2013
    Manufacturer
    WRIGHT MEDICAL TECHNOLOGY, INC.
    Product Code
    KWA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE INVESTIGATION IS NOT COMPLETE. TRENDS WILL BE EVALUATED. THE EVENT CODE IS ADDRESSED IN THE PACKAGE INSERT. THIS REPORT WILL BE UPDATED WHEN THE INVESTIGATION IS COMPLETE. THIS IS THE SAME EVENT AS 1043534-2013-01180, 01181, 01182.

    Description of Event or Problem · 1

    ALLEGEDLY REVISED DUE TO MOM COMPLICATIONS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    340113 CONSERVE(R) PLUS HA CUP HIP COMPONENT, CODE:KWA KWA WRIGHT MEDICAL TECHNOLOGY, INC. 096370922

    Patients

    Seq Age Sex Outcome Treatment
    1 78 YR Required Intervention