BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2140861 · Received May 31, 2011

    Report

    Report Number
    1824206-2011-02980
    Event Type
    Malfunction
    Date Received
    May 31, 2011
    Date of Event
    May 10, 2011
    Report Date
    May 10, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT REPLACED THE COILED CABLE BUT THE ISSUE REMAINED. THE ACCOUNT'S ENGINEER FOUND THE POWER SUPPLY BOARD WAS ONLY GIVING A BATTERY CHARGE OF 9 VOLTS. HE REPLACED THE POWER SUPPLY BOARD TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE BED HAS AN 8 FLASH CODE. THE ACCOUNT FOUND THE LEFT COILED CABLE WAS FRAYED AND BARE WIRES WERE EXPOSED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

    Patients

    Seq Age Sex Outcome Treatment
    1