BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 3761332 · Received January 2, 2014

    Report

    Report Number
    1824206-2014-00011
    Event Type
    Malfunction
    Date Received
    January 2, 2014
    Date of Event
    December 16, 2013
    Report Date
    December 16, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND FLUID HAD SPILLED IN THE SIDE RAIL LATCHING MECHANISM. THE TECHNICIAN CLEANED THE FLUID OUT OF THE SIDE RAIL LATCH AND LUBRICATED ALL PARTS OF THE SIDE RAIL TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE SIDE RAIL DOES NOT LATCH. NO PT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1252 TOTALCARE BED A/C POWERED ADJUSTABLE HOSP BED FNL HILL-ROM, INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1