BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    MDR report key: 4222555 · Received November 4, 2014

    Report

    Report Number
    3008262382-2014-01821
    Event Type
    Malfunction
    Date Received
    November 4, 2014
    Report Date
    October 14, 2014
    Manufacturer
    INVACARE REHABILITATION EQUIP
    Product Code
    CAW
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    PER INDEPENDENT REPAIR CENTER, THE UNIT HAD LOW O2 OR YELLOW LIGHT. THE KEY FAILURE WAS THE PE VALVE TO THE SIEVE BED/PRODUCT TANK STICKING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    705213 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE REHABILITATION EQUIP IRC5PO2

    Patients

    Seq Age Sex Outcome Treatment
    1 Other