BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 2843612 · Received October 24, 2012

    Report

    Report Number
    1824206-2012-06814
    Event Type
    Malfunction
    Date Received
    October 24, 2012
    Date of Event
    October 8, 2012
    Report Date
    October 8, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    HILL-ROM TECHNICIAN FOUND A LARGE AMOUNT OF DRIED LIQUID MATERIAL PREVENTING THE SIDE RAIL FROM LATCHING. HE REMOVED AND CLEANED THE SIDERAIL TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATED THE RIGHT SIDE RAIL WILL NOT LATCH IN THE UP POSITION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1