BEUDAMED
    FDA Adverse Event Death Summary report: N

    HIGH/LOW BATH

    MDR report key: 297170 · Received September 25, 2000

    Report

    Report Number
    9611530-2000-00037
    Event Type
    Death
    Date Received
    September 25, 2000
    Date of Event
    January 1, 2000
    Report Date
    September 12, 2000
    Manufacturer
    ARJO HOSPITAL EQUIPMENT AB
    Product Code
    ILJ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NL
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    THE FACILITY REPORTS THE PT FILLED THE TUB WITH HOT WATER. THE PT WAS BURNED BY THE TOO HOT WATER AND DIED SOON THEREAFTER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HIGH/LOW BATH BATHING SYSTEM ILJ ARJO HOSPITAL EQUIPMENT AB ATBXXXX NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Death