BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2232677 · Received July 19, 2011

    Report

    Report Number
    1824206-2011-03810
    Event Type
    Malfunction
    Date Received
    July 19, 2011
    Date of Event
    July 1, 2011
    Report Date
    July 1, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    REPAIRS HAVE NOT BEEN COMPLETED.

    Description of Event or Problem · 1

    THE ACCOUNTS MAINTENANCE STATED THREE OF THE SIDERAILS WILL NOT LATCH IN THE UP POSITION. WHEN HE OPENED THE SIDERAIL CENTER ARM HE FOUND THE SIDERAIL UPGRADE WAS NOT DONE.

    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