BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NEXGEN LPS-FLEX OPTION FEMORAL COMPONENT

    MDR report key: 3962601 · Received July 15, 2014

    Report

    Report Number
    3007963827-2014-00029
    Event Type
    Injury
    Date Received
    July 15, 2014
    Report Date
    June 16, 2014
    Manufacturer
    ZIMMER
    Product Code
    NJL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    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 THE PATIENT IS EXPERIENCING PAIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    412261 NEXGEN LPS-FLEX OPTION FEMORAL COMPONENT NJL ZIMMER 61944860

    Patients

    Seq Age Sex Outcome Treatment
    1 Other