BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    MDR report key: 4094054 · Received September 16, 2014

    Report

    Report Number
    1031452-2014-09482
    Event Type
    Malfunction
    Date Received
    September 16, 2014
    Report Date
    August 25, 2014
    Manufacturer
    INVACARE FLORIDA OPERATIONS
    Product Code
    CAW
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    PER PROVIDER THE VALVE IS STUCK. PER THE INDEPENDENT REPAIR CENTER STATEMENT THERE IS ALARMING OR RED LIGHT. THE SIEVE BEDS IS SATURATED. THE EXHAUST MANIFOLD ASSY VALVE IS STUCK. THE EXAUST MUFFLER IS LEAKING, THE TY WRAPS TUBING ARE LEAKING AND THE GEAR CLAMPS ON TUBING IS LEAKING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    571198 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

    Patients

    Seq Age Sex Outcome Treatment
    1 Other