BEUDAMED
    FDA Adverse Event Other Summary report: N

    DIAL FLOWMETER

    MDR report key: 220372 · Received April 19, 1999

    Report

    Report Number
    2523148-1999-00003
    Event Type
    Other
    Date Received
    April 19, 1999
    Date of Event
    April 5, 1999
    Report Date
    April 5, 1999
    Manufacturer
    PRECISION MEDICAL, INC.
    Product Code
    CAN
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT NURSE USED DIAL FLOWMETER INCORRECTLY. TREATMENT REQUIRED 7 "LPM" SO USER SET THE FLOW BETWEEN THE 6 AND 8 "LPM" DETENT SETTINGS AND THE PO2 DROPPED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DIAL FLOWMETER OXYGEN DIAL FLOWMETER CAN PRECISION MEDICAL, INC. 7MFA NI

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention