BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    MDR report key: 4122684 · Received September 26, 2014

    Report

    Report Number
    1031452-2014-11201
    Event Type
    Malfunction
    Date Received
    September 26, 2014
    Report Date
    September 8, 2014
    Manufacturer
    INVACARE FLORIDA OPERATIONS
    Product Code
    CAW
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    PER INDEPENDENT REPAIR CENTER, UNIT IS ALARMING OR RED LIGHT. FAILURES INCLUDE: THE SIEVE BEDS LEAKING, PILOT VALVE STUCK, NOISY COMPRESSOR, LEAKING AT THE HOSE CLAMP, LEAKING AT THE O-RING, LEAKING AT THE ZIP TIES, DIRTY MUFFLER, DIRTY PM KIT, AND NO ALARM ON THE POWER SWITCH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    602130 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

    Patients

    Seq Age Sex Outcome Treatment
    1 Other