BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2241337 · Received September 2, 2011

    Report

    Report Number
    1824206-2011-04618
    Event Type
    Malfunction
    Date Received
    September 2, 2011
    Date of Event
    August 15, 2011
    Report Date
    August 15, 2011
    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 RIGHT HEAD SIDERAIL LATCH WOULD NOT SPRING BACK DUE TO FLUID IN THE LATCH ASSEMBLY. HE CLEANED AND LUBRICATED THE SIDERAIL LATCH ASSEMBLY TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT STATED THE SIDERAIL WOULD NOT LATCH.

    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