BEUDAMED
    FDA Adverse Event Other Summary report: N

    AMBULIFT BSQ

    MDR report key: 287036 · Received July 26, 2000

    Report

    Report Number
    9617021-2000-00130
    Event Type
    Other
    Date Received
    July 26, 2000
    Date of Event
    April 4, 2000
    Report Date
    July 24, 2000
    Manufacturer
    ARJO LTD.
    Product Code
    FSA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE FACILITY REPORTS THE CLIENT HAD BEEN BATHED. THE CARER WAS ATTEMPTING TO RAISE THE PT OUT OF THE BATH WHEN THE CHAIR BECAME DETACHED. THE CLIENT AND CHAIR FELL BACK INTO THE BATH. THE CLIENT WAS SHAKEN AND THEIR ARTHIRITIC KNEE WAS CAUSING THEM PAIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AMBULIFT BSQ PATIENT LIFT FSA ARJO LTD. ABXXXX NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other