BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2033151 · Received February 28, 2011

    Report

    Report Number
    1824206-2011-01168
    Event Type
    Malfunction
    Date Received
    February 28, 2011
    Date of Event
    February 4, 2011
    Report Date
    February 4, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT REQUESTED A REPLACEMENT LATCH, LATCH SPRING AND D-PIN. REPAIRS HAVE NOT BEEN COMPLETED.

    Description of Event or Problem · 1

    INFO REC'D INDICATES AFTER RELEASING ONE OF THE HEAD SIDERAILS THE LATCH WILL NOT RETURN TO ITS POSITION AND THEREFORE THE SIDERAIL WILL NOT LATCH IN THE UP POSITION.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1