BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2112439 · Received April 28, 2011

    Report

    Report Number
    1824206-2011-02442
    Event Type
    Malfunction
    Date Received
    April 28, 2011
    Date of Event
    April 5, 2011
    Report Date
    April 6, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND SOMETHING LEAKED INTO THE SIDERAIL CENTER ARM, CAUSING THE LATCH TO STICK OPEN. THE TECHNICIAN CLEANED THE SIDERAIL CENTER ARM ASSEMBLY TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE LEFT HEAD SIDERAIL IS NOT LATCHING.

    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