BEUDAMED
    FDA Adverse Event Summary report: N

    FLOW SELECTOR

    MDR report key: 68221 · Received January 6, 1997

    Report

    Report Number
    68221
    Date Received
    January 6, 1997
    Date of Event
    December 9, 1996
    Report Date
    January 6, 1997
    Manufacturer
    MEDICAL FITTINGS, INC.
    Product Code
    CAX
    Report Source
    User Facility report
    Reporter Location
    VA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PT WAS ON OXYGEN. RESPIRATORY THERAPY WAS CALLED TO SET UP PT ON CONTINUOUS OXIMETER. PT FOUND BY RESPIRATORY WITHOUT OXYGEN RELATED TO IMPROPER OXYGEN SETUP. SPO2 55% ON ROOM AIR. PT WAS CYANOTIC WITH LABORED RESPIRATIONS. PT HOOKED UP ON O2 PROPERLY BY RESPIRATORY THERAPY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLOW SELECTOR FLOW SELECTOR CAX MEDICAL FITTINGS, INC. MF 8025 *

    Patients

    Seq Age Sex Outcome Treatment
    1 80 YR