BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    MDR report key: 4068340 · Received September 8, 2014

    Report

    Report Number
    1031452-2014-08481
    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. PER INDEPENDENT REPAIR CENTER STATEMENT THE UNIT IS ALARMING OR RED LIGHT. ADDITIONAL MALFUNCTIONS ARE 1101141 4 WAY VALVE ALARMING. 1161257 SIEVE BED LOW O2: PEV ALARMING AND PILOT VALVE ALARMING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    548792 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2

    Patients

    Seq Age Sex Outcome Treatment
    1 Other