BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RESIDENT BED

    MDR report key: 3060506 · Received March 25, 2013

    Report

    Report Number
    1824206-2013-01660
    Event Type
    Malfunction
    Date Received
    March 25, 2013
    Date of Event
    February 25, 2013
    Report Date
    February 25, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE RELAY WAS STUCK. THE TECHNICIAN TAPPED ON THE RELAY AND THE HEAD FUNCTION STARTED TO WORK AND HE COULD NOT GET THE PROBLEM TO REOCCUR. THE TECHNICIAN EXPLAINED TO THE ACCOUNT THAT THEY SHOULD REPLACE THE CONTROL BOX IF THE PROBLEM WERE TO REOCCUR.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE HEAD OF THE BED IS STUCK IN THE RAISED POSITION. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    121375 RESIDENT BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 870

    Patients

    Seq Age Sex Outcome Treatment
    1