BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PROFEMUR MODULAR FEMORAL NECK

    MDR report key: 8853674 · Received August 1, 2019

    Report

    Report Number
    3010536692-2019-00979
    Event Type
    Injury
    Date Received
    August 1, 2019
    Report Date
    March 31, 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 · 0

    SEE ATTACHED. - ATTACHMENT: [RIPOJULY2019SIGNED.PDF].

    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 50 PPR67250 LOT T06123347. TIGE "ANCA FIT?" REV. HAP 1/3 PROXIMAL 13D PPR67612 LOT T07126098. INSERT CERAM "ANCA FIT?" 28/40 50-52-54/28 AL2.O3 BIO. FORTE PPR67510 LOT T07129760.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    647661 PROFEMUR MODULAR FEMORAL NECK HIP COMPONENT LWJ MICROPORT ORTHOPEDICS INC. PHA01252 T09128532

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Required Intervention