BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECA

    MDR report key: 5147788 · Received October 14, 2015

    Report

    Report Number
    5147788
    Event Type
    Malfunction
    Date Received
    October 14, 2015
    Date of Event
    September 28, 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

    WHEN A PATIENT IS WEIGHED IT IS DIFFICULT FOR THE STAFF TO NAVIGATE FROM POUNDS TO KILOS OR VICE VERSA. STAFF ALWAYS THINK THIS DEVICE IS BROKEN BECAUSE THEY CANNOT NAVIGATE THE MENU. NEEDS TO HAVE BETTER INSTRUCTION ON HOW TO NAVIGATE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    678367 SECA SCALE FRW SECA CORP. 644

    Patients

    Seq Age Sex Outcome Treatment
    1