BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NEXGEN LPS-FLEX GSF FEMORL COMPONENET

    MDR report key: 4023553 · Received August 14, 2014

    Report

    Report Number
    3007963827-2014-00039
    Event Type
    Injury
    Date Received
    August 14, 2014
    Report Date
    July 18, 2014
    Manufacturer
    ZIMMER ORTHOPEDIC MFG LTD
    Product Code
    JWH
    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
    486847 NEXGEN LPS-FLEX GSF FEMORL COMPONENET JWH ZIMMER ORTHOPEDIC MFG LTD 61515797

    Patients

    Seq Age Sex Outcome Treatment
    1 Other