BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    MDR report key: 4242113 · Received November 11, 2014

    Report

    Report Number
    1031452-2014-18248
    Event Type
    Malfunction
    Date Received
    November 11, 2014
    Report Date
    October 20, 2014
    Manufacturer
    INVACARE FLORIDA OPERATIONS
    Product Code
    CAW
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    INDEPENDENT REPAIR CENTER: ALLEGED KEY FAILURE LEAKING. ALARMING OR RED LIGHT. ZIP TIE/SIEVEBED ISSUES. FILTER DIRTY. SIEVEBEDS LEAKING (KEY). MANIFOLD HEAT EXCHANGER REPLACED. MANIFOLD ASSEMBLY - STUCK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    725395 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

    Patients

    Seq Age Sex Outcome Treatment
    1 Other