BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BUR

    MDR report key: 3840172 · Received May 23, 2014

    Report

    Report Number
    MW5036323
    Event Type
    Injury
    Date Received
    May 23, 2014
    Date of Event
    May 5, 2014
    Report Date
    May 22, 2014
    Manufacturer
    STRYKER
    Product Code
    HTT
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    BUR BROKE DURING PROCEDURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    307085 BUR BUR HTT STRYKER OVAL BUR

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR Required Intervention