BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    840 VENTILATOR

    MDR report key: 3872294 · Received April 18, 2014

    Report

    Report Number
    8020893-2014-00944
    Event Type
    Malfunction
    Date Received
    April 18, 2014
    Report Date
    March 20, 2014
    Manufacturer
    COVIDIEN, FORMERLY NELLCOR
    Product Code
    CBK
    PMA / PMN Number
    K970460
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THE CUSTOMER SUPPORT ENGINEER (CSE) VERIFIED THE MALFUNCTION. THE CSE INSPECTED THE DEVICE AND REPLACED THE GRAPHICAL USER INTERFACE (GUI) PRINTED CIRCUIT BOARD (PCB) AND THE BACKLIGHT INVERTER PCB. THE DEVICE PASSED EXTENDED SELF-TEST, SHORT SELF-TEST, AND THE PERFORMANCE VERIFICATION TEST. COVIDIEN REF: (B)(4).

    Description of Event or Problem · 1

    A REPORT WAS RECEIVED FROM THE USA WITH INFO THAT AN 840 VENTILATOR HAD AN UPPER ERRATIC GRAPHICAL USER INTERFACE (GUI) DISPLAY. INFO RECEIVED INDICATED THE EVENT DID NOT OCCUR DURING PT USE. THE DATE OF THE EVENT WAS NOT PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    238418 840 VENTILATOR CBK COVIDIEN, FORMERLY NELLCOR 840

    Patients

    Seq Age Sex Outcome Treatment
    1