BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SCALE

    MDR report key: 5155733 · Received October 16, 2015

    Report

    Report Number
    5155733
    Event Type
    Malfunction
    Date Received
    October 16, 2015
    Date of Event
    September 29, 2015
    Report Date
    September 29, 2015
    Manufacturer
    SECA CORP.
    Product Code
    FRW
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Description of Event or Problem · 1

    THE SCALE IS JUST OVERLY SENSITIVE AS FAR AS BEING ON A BALANCED FLOOR. YOU CAN LEVEL IT BUT IF IT GETS MOVED JUST A HAIR IT THROWS IT OFF. IT IS TO THE POINT WHERE THE HOSPITAL REFUSES TO EVEN USE THE SCALE ANY MORE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    687851 SCALE FRW SECA CORP. 644

    Patients

    Seq Age Sex Outcome Treatment
    1 NO