BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    840 VENTILATOR

    MDR report key: 2903790 · Received January 4, 2013

    Report

    Report Number
    8020893-2013-00023
    Event Type
    Malfunction
    Date Received
    January 4, 2013
    Date of Event
    December 4, 2012
    Report Date
    December 5, 2012
    Manufacturer
    COVIDIEN, FORMERLY NELLCOR
    Product Code
    CBK
    PMA / PMN Number
    K970460
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    CUSTOMER REPORTED THAT THE 840 VENTILATOR HAS AN ERRATIC SCREEN. NO PT INVOLVEMENT. COVIDIEN INSPECTED THE DEVICE AND COULD DUPLICATE THE ALLEGED MALFUNCTION. THE VENTILATOR PASSED ALL TESTING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    5258 840 VENTILATOR VENTILATOR CBK COVIDIEN, FORMERLY NELLCOR 840

    Patients

    Seq Age Sex Outcome Treatment
    1