BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BARIATRIC

    MDR report key: 2091073 · Received May 12, 2011

    Report

    Report Number
    1824206-2011-02658
    Event Type
    Malfunction
    Date Received
    May 12, 2011
    Date of Event
    April 11, 2011
    Report Date
    April 11, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN STRAIGHTENED THE SIDERAIL LATCH COVER TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO REC'D INDICATES THE METAL SIDERAIL LATCH COVER IS BENT, CATCHING THE LATCH AND PREVENTING THE SIDERAIL LATCH FROM ENGAGING. SIDERAIL WILL NOT LATCH.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK