BEUDAMED
    FDA Adverse Event Other Summary report: N

    PRECISION

    MDR report key: 3986980 · Received August 4, 2014

    Report

    Report Number
    MW5037655
    Event Type
    Other
    Date Received
    August 4, 2014
    Date of Event
    July 2, 2014
    Report Date
    August 1, 2014
    Manufacturer
    PRECISON MEDICAL
    Product Code
    CAX
    Report Source
    Voluntary report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    PATIENT ON O2 VIA OXYGEN FLOW METER. THE OXYGEN FLOW SELECTOR WAS TURNED TO THE WRONG PORT, OFF INSTEAD OF ON. RT ASSISTING PATIENT FOUND PATIENT DESAT AT 85%. RT ADJUSTED OXYGEN FLOW SELECTOR TO THE CORRECT PORT AND O2 STAT WENT UP TO 97%.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    455114 PRECISION FLOW SELECTOR CAX PRECISON MEDICAL PM1000

    Patients

    Seq Age Sex Outcome Treatment
    1 74 YR