BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MODULAR NAIL

    MDR report key: 125443 · Received October 7, 1997

    Report

    Report Number
    125443
    Event Type
    Injury
    Date Received
    October 7, 1997
    Date of Event
    August 29, 1997
    Report Date
    October 6, 1997
    Manufacturer
    SMITH & NEPHEW, INC./ORTHOPAEDICS DIV.
    Product Code
    MQZ
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    IA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE NAIL, INITIALLY IMPLANTED ON 1/29/96, WAS REMOVED ON 8/29/97 DUE TO A COMPLAINT OF PAIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MODULAR NAIL Implant TRAUMA MQZ SMITH & NEPHEW, INC./ORTHOPAEDICS DIV. NA NI

    Patients

    Seq Age Sex Outcome Treatment
    1 37 YR Hospitalization| R