BEUDAMED
    FDA Adverse Event Death Summary report: N

    NIBP HOSE

    MDR report key: 340880 · Received July 6, 2001

    Report

    Report Number
    3023361-2001-00001
    Event Type
    Death
    Date Received
    July 6, 2001
    Date of Event
    July 2, 2001
    Report Date
    July 3, 2001
    Manufacturer
    UNK
    Product Code
    DXN
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    LA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    USER ALLEGED THAT THEY CONNECTED THE NIBP HOSE TO THE HEPLOC CONNECTOR ON AN IV INSTEAD OF THE CUFF.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    30365 NIBP HOSE NIBP ACCESSORY DXN UNK UNK NA

    Patients

    Seq Age Sex Outcome Treatment
    1 Death 90467 NIBP MODULE, NIBP CUFF - BRANDED 'LORIN| MEDICAL'.