BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BARREL BUR

    MDR report key: 217676 · Received April 1, 1999

    Report

    Report Number
    1811755-1999-00010
    Event Type
    Malfunction
    Date Received
    April 1, 1999
    Date of Event
    March 3, 1999
    Report Date
    March 3, 1999
    Manufacturer
    STRYKER INSTRUMENTS
    Product Code
    HTT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    BUR BROKE DURING PROCEDURE AT LEVEL OF J-NOTCH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BARREL BUR BUR HTT STRYKER INSTRUMENTS 1607002001S1 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN