BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNKNOWN ZIMMER NAIL

    MDR report key: 5250298 · Received November 25, 2015

    Report

    Report Number
    1822565-2015-02458
    Event Type
    Injury
    Date Received
    November 25, 2015
    Date of Event
    October 31, 2015
    Report Date
    October 29, 2015
    Manufacturer
    ZIMMER INC
    Product Code
    HAO
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THIS REPORT WILL BE AMENDED WHEN OUR INVESTIGATION IS COMPLETE.

    Description of Event or Problem · 1

    IT IS REPORTED THE PATIENT WAS REVISED DUE TO A BROKEN NAIL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    780477 UNKNOWN ZIMMER NAIL TRAUMA PROSTHESIS HAO ZIMMER INC

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention