BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    MDR report key: 4003842 · Received August 12, 2014

    Report

    Report Number
    1031452-2014-05746
    Event Type
    Malfunction
    Date Received
    August 12, 2014
    Report Date
    July 1, 2014
    Manufacturer
    INVACARE FLORIDA OPERATIONS
    Product Code
    CAW
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    DURING TESTING AND REPAIR AT THE INDEPENDENT REPAIR CENTER, THE (B)(4) CONCENTRATOR POWER SWITCH HAS NO ALARM. THIS WAS DUE TO A DEFECTIVE POWER SWITCH WHICH LED TO THE MALFUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    478644 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

    Patients

    Seq Age Sex Outcome Treatment
    1 Other