BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NEXGEN CRUCIATE RETAINING FLEX FEMORAL

    MDR report key: 2020431 · Received February 8, 2011

    Report

    Report Number
    1822565-2011-00183
    Event Type
    Malfunction
    Date Received
    February 8, 2011
    Report Date
    January 12, 2011
    Manufacturer
    ZIMMER, INC.
    Product Code
    JWH
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ND, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS REPORT WILL BE AMENDED WHEN OUR INVESTIGATION IS COMPLETE.

    Description of Event or Problem · 1

    IT IS REPORTED THAT X-RAYS SHOW SIGNS OF RADIOLUCENCY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NEXGEN CRUCIATE RETAINING FLEX FEMORAL JWH ZIMMER, INC. 61439610

    Patients

    Seq Age Sex Outcome Treatment
    1