BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PARKER BATH

    MDR report key: 1304010 · Received January 6, 2009

    Report

    Report Number
    9611530-2008-00075
    Event Type
    Malfunction
    Date Received
    January 6, 2009
    Date of Event
    November 8, 2008
    Report Date
    January 6, 2009
    Manufacturer
    ARJO HOSPITAL EQUIPMENT AB
    Product Code
    ILJ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK

    Narratives

    Description of Event or Problem · 1

    THE FACILITY REPORTED AFTER THE BATH FOOTWELL WAS FILLED WITH WATER, THE PATIENT WAS PLACED IN THE BATH USING THE OVERHEAD HOIST. THERE WAS A CREAKING NOISE AND A BANG AND THE TUB BECAME UNSTABLE. THE PATIENT WAS LIFTED FROM THE TUB. THERE WERE NO INJURIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PARKER BATH BATHING SYSTEM ILJ ARJO HOSPITAL EQUIPMENT AB

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention