BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2220480 · Received July 18, 2011

    Report

    Report Number
    1824206-2011-03766
    Event Type
    Malfunction
    Date Received
    July 18, 2011
    Date of Event
    June 28, 2011
    Report Date
    June 28, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    HI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THAT THE VALVE SOLENOID WAS FAILING. REPLACED THE VALVE SOLENOID TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    FACILITY ALLEGED THAT THE HEAD UP WAS NOT WORKING. NO INJURIES REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P1900

    Patients

    Seq Age Sex Outcome Treatment
    1