BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    4 MOTOR ADVANCE BED

    MDR report key: 1122218 · Received August 15, 2008

    Report

    Report Number
    1824206-2008-03132
    Event Type
    Malfunction
    Date Received
    August 15, 2008
    Date of Event
    July 15, 2008
    Report Date
    July 15, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE HOSPITAL MAINTENANCE PERSON REPORTED THAT THE HEAD FUNCTION RAN UP UNINTENTIONALLY. HE FOUND THAT THE HEAD UP PATIENT SWITCH WAS STUCK IN THE LEFT HEAD SIDERAIL. HE REPLACED THE SWITCH ASSEMBLY AND THE BED FUNCTIONED AS DESIGNED. HE STATED THAT THERE WERE NO INJURIES ASSOCIATED WITH THIS PRODUCT MALFUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 4 MOTOR ADVANCE BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1105 NA

    Patients

    Seq Age Sex Outcome Treatment
    1