BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PROFEMUR® MODULAR FEMORAL NECK

    MDR report key: 8848834 · Received July 31, 2019

    Report

    Report Number
    3010536692-2019-00931
    Event Type
    Injury
    Date Received
    July 31, 2019
    Report Date
    February 6, 2020
    Manufacturer
    MICROPORT ORTHOPEDICS INC.
    Product Code
    LWJ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IT
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THIS EVENT WILL BE UPDATED WHEN INVESTIGATION IS COMPLETE.

    Description of Event or Problem · 1

    ALLEGEDLY, PATIENT WAS REVISED DUE TO PROSTHESIS DISLOCATION .COMPONENTS NOT REVISED : COTYLE "ANCA" AVEC TROUS A/REVET. HAP 52 PPR67252 LOT R0693669; TIGE "ANCA FIT?" REV. HAP 1/3 PROXIMAL 15G PPR67622 LOT R0591067.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    639967 PROFEMUR® MODULAR FEMORAL NECK HIP COMPONENT LWJ MICROPORT ORTHOPEDICS INC. PHA01242 R0693877.1

    Patients

    Seq Age Sex Outcome Treatment
    1 79 YR Required Intervention