BEUDAMED
    FDA Adverse Event Death Summary report: N

    OXINET II CENTRAL STATION

    MDR report key: 385604 · Received April 2, 2002

    Report

    Report Number
    2025525-2002-00003
    Event Type
    Death
    Date Received
    April 2, 2002
    Date of Event
    March 5, 2002
    Report Date
    March 5, 2002
    Manufacturer
    NELLCOR PURITAN BENNETT
    Product Code
    DQA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IN 03/2002 NELLCOR PURITAN BENNETT REC'D A CALL TO INQUIRE ABOUT DOWNLOADING TREND INFO ON AN OXINET II CENTRAL STATION. ACCORDING TO THE CUSTOMER THE PT EXPIRED AND THE N-3000 PULSE OXIMETER WAS ALARMING AT BEDSIDE BUT NOT AT THE CENTRAL STATION. ACCORDING TO THE CUSTOMER, ONE OF THE NURSES "FIDDLED" THE OXINET CABLE AND THE CENTRAL STATION STARTED ALARMING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OXINET II CENTRAL STATION CENTRAL STATION DQA NELLCOR PURITAN BENNETT OXINET II SYSTEM NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Death