BEUDAMED
    FDA Adverse Event Death Summary report: N

    TIMETER

    MDR report key: 376017 · Received February 7, 2002

    Report

    Report Number
    376017
    Event Type
    Death
    Date Received
    February 7, 2002
    Date of Event
    January 30, 2002
    Report Date
    February 7, 2002
    Manufacturer
    UNK
    Product Code
    CAN
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    TX, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PT FOUND UNRESPONSIVE, BUT BREATHING ON THEIR OWN. MD SUSPECTED INCREASED O2 FLOW BASED ON ABG'S. SUSPECTS INCREASED O2 KNOCKED OUT THE PT'S HYPOXIC DRIVE. INTUBATED AND SENT TO ICU. O2 WAS AT 36. TRIED FLOWMETER IN ANOTHER ROOM - TURNED OFF AND IT CONTINUED TO REGISTER 36. TRIED IN 3RD ROOM WITH SAME RESULTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TIMETER OXYGEN FLOWMETER CAN UNK * *

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR Death