BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE-

    MDR report key: 2023153 · Received February 15, 2011

    Report

    Report Number
    1824206-2011-00884
    Event Type
    Malfunction
    Date Received
    February 15, 2011
    Date of Event
    February 1, 2011
    Report Date
    February 1, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THE BED IN THE BED SHOP. FOUND - THE HEAD SECTION WOULD NOT GO UP. NO ALARMS. THE HEAD SECTION WAS FLAT AND WOULD NOT GO UP ABOVE 30 DEGREES. THE BATTERY LED WAS LIT. THE HEAD SECTION WOULD NOT RAISE MANUALLY OR WITH THE SIDERAIL CONTROLS. CAUSE - THE HEAD UP VALVE IS STUCK. REPLACED THE HEAD UP VALVE TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    COMPLAINT ALLEGED THAT THE HEAD SECTION WOULD NOT GO UP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE- AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1900C001742-1

    Patients

    Seq Age Sex Outcome Treatment
    1