BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RUSCH GREENSPEC FO BLADE, MILLER 3

    MDR report key: 3113866 · Received May 7, 2013

    Report

    Report Number
    3004365956-2013-00150
    Event Type
    Malfunction
    Date Received
    May 7, 2013
    Date of Event
    March 4, 2013
    Report Date
    April 12, 2013
    Manufacturer
    TELEFLEX MEDICAL
    Product Code
    CAL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE SAMPLE WAS RECEIVED BY THE MANUFACTURER, BUT THE INVESTIGATION IS INCOMPLETE AT THE TIME OF THIS REPORT.

    Description of Event or Problem · 1

    THE COMPLAINT WAS REPORTED AS: THE BLADES ARE STICKING TO THE HANDLES AND NOT DIS-ARTICULATING. NO REPORT OF PATIENT INJURY. NO REPORT OF PATIENT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    198046 RUSCH GREENSPEC FO BLADE, MILLER 3 FIBEROPTIC LARYNGOSCOPE BLADE CAL TELEFLEX MEDICAL

    Patients

    Seq Age Sex Outcome Treatment
    1