BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    MDR report key: 4067085 · Received September 8, 2014

    Report

    Report Number
    1031452-2014-08448
    Event Type
    Malfunction
    Date Received
    September 8, 2014
    Report Date
    August 15, 2014
    Manufacturer
    INVACARE FLORIDA OPERATIONS
    Product Code
    CAW
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    PER PROVIDER THE UNIT IS ALARMING. REPLACED PILOT VALVE. PER INDEPENDENT REPAIR CENTER STATEMENT THE UNIT IS ALARMING OR RED LIGHT. ADDITIONAL MALFUNCTIONS 1143497 PILOT VALVE ALARMING AND 2001134 POWER SWITCH HAS NO ALARM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    548286 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

    Patients

    Seq Age Sex Outcome Treatment
    1 Other