BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 2232645 · Received July 19, 2011

    Report

    Report Number
    1824206-2011-03794
    Event Type
    Malfunction
    Date Received
    July 19, 2011
    Date of Event
    July 6, 2011
    Report Date
    July 7, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THAT THE SIDERAIL WILL NOT LATCH AS THE MOUNTING BRACKET WAS BENT. REPLACED THE ENTIRE RAIL TO RESOLVE THIS ISSUE. BED FOUND IN THE BASEMENT.

    Description of Event or Problem · 1

    COMPLAINANT ALLEGED THAT THE SIDERAIL WILL NOT LATCH. NO INJURY ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P3200

    Patients

    Seq Age Sex Outcome Treatment
    1