BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 1993160 · Received January 21, 2011

    Report

    Report Number
    1824206-2011-00403
    Event Type
    Malfunction
    Date Received
    January 21, 2011
    Date of Event
    December 29, 2010
    Report Date
    December 29, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT'S MAINTENANCE REPLACED THE LEFT COILED CABLE TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED, THE PUMP IS NOT WORKING. HE FOUND BARE WIRES ON THE LEFT COILED CABLE.

    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