BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BASICCARE ELECTRIC BED

    MDR report key: 3074993 · Received April 18, 2013

    Report

    Report Number
    1824206-2013-02261
    Event Type
    Malfunction
    Date Received
    April 18, 2013
    Date of Event
    March 25, 2013
    Report Date
    March 25, 2013
    Manufacturer
    OPTIMA HEALTHCARE, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    TH
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ALLEGED PROBLEM WAS A STUCK HEAD UP SWITCH IN THE FOOT END CONTROL PANEL. UNPLUGGING THE FOOT END CONTROL PANEL CABLE FROM THE CONTROL BOX CORRECTED THE ISSUE. A REPLACEMENT CONTROL PANEL WAS REQUESTED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THAT THE BED EXPERIENCED AN UNINTENTIONAL MOVEMENT OF THE HEAD UP FUNCTION. THERE WERE NO INJURIES ASSOCIATED WITH THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    168516 BASICCARE ELECTRIC BED AC POWERED ADJUSTABLE HOSPITAL BED FNL OPTIMA HEALTHCARE, INC. 1440

    Patients

    Seq Age Sex Outcome Treatment
    1