BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BARIATRIC

    MDR report key: 1864387 · Received October 4, 2010

    Report

    Report Number
    1824206-2010-10271
    Event Type
    Malfunction
    Date Received
    October 4, 2010
    Date of Event
    September 9, 2010
    Report Date
    September 9, 2010
    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 THE LOCK LATCH COVER WAS BENT UNDERNEATH THE LOCKING MECHANISM WHICH PREVENTED THE SIDERAIL FROM LOCKING PROPERLY. THE TECHNICIAN ADJUSTED THE BENT LOCK LATCH COVER TO CORRECT THE PROBLEM.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE RIGHT FOOT SIDERAIL FAILED TO MOVE INTO THE RAISED LOCKED POSITION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE BARIATRIC AC POWERED HOSPITAL BED FNL HILL-ROM, INC. 1840

    Patients

    Seq Age Sex Outcome Treatment
    1