BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1930581 · Received December 1, 2010

    Report

    Report Number
    1824206-2010-11338
    Event Type
    Malfunction
    Date Received
    December 1, 2010
    Date of Event
    November 5, 2010
    Report Date
    November 5, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE SIDERAIL LATCHING ASSEMBLY WAS FULL OF BLOOD AND GUMMED UP. HE CLEANED AND DISINFECTED THE SIDERAIL LATCH ASSEMBLY TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO REC'D INDICATES THE LEFT FOOT SIDERAIL IS NOT LATCHING CONSISTENTLY.

    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