BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2142624 · Received June 21, 2011

    Report

    Report Number
    1824206-2011-03367
    Event Type
    Malfunction
    Date Received
    June 21, 2011
    Date of Event
    June 7, 2011
    Report Date
    June 7, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MS, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THAT THE D-RING WAS MISSION FROM LATCH PIN. REPOSITIONED PIN AND REPLACED THE D-RING TO RESOLVE THIS ISSUE. BED FOUND IN ICU2.

    Description of Event or Problem · 1

    FACILITY ALLEGED THAT ONE OF THE SIDERAILS WILL LATCH AND THEN COME DOWN IF IT IS BUMPED. NO INJURY ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. PR1900

    Patients

    Seq Age Sex Outcome Treatment
    1