BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 2172446 · Received June 17, 2011

    Report

    Report Number
    1824206-2011-03312
    Event Type
    Malfunction
    Date Received
    June 17, 2011
    Date of Event
    May 31, 2011
    Report Date
    May 31, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT REPLACED THE BRIDGE RECTIFIER TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT STATED THEY HAVE A BED IN STORAGE AND FOUND THE BED HAS NO POWER. WHEN HE PLUGGED THE BED INTO AC POWER, HE SAW A SMALL PUFF OF SMOKE COMING FROM THE TRANSFORMER AREA. HE FOUND 120 AC INTO THE TRANSFORMER AND 18 VAC OUT FROM THE TRANSFORMER, BUT 0 VDC.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1