BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 1850097 · Received September 28, 2010

    Report

    Report Number
    1824206-2010-10169
    Event Type
    Malfunction
    Date Received
    September 28, 2010
    Date of Event
    August 31, 2010
    Report Date
    August 31, 2010
    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 DRIED FLUIDS IN THE SIDERAIL CENTER ARM. THE TECHNICIAN CLEANED AND REASSEMBLED THE SIDERAIL CENTER ARM TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES, THE RIGHT SIDERAIL WILL NOT LATCH.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1