BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1851402 · Received September 23, 2010

    Report

    Report Number
    1824206-2010-10018
    Event Type
    Malfunction
    Date Received
    September 23, 2010
    Date of Event
    August 30, 2010
    Report Date
    June 16, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH FOUND THE UNIT LOW ON HYDRAULIC FLUID REFILLED HYDRAULIC FLUID, THAT DID NOT RESOLVE THE ISSUE. UPON FURTHER INVESTIGATION IN THE WAREHOUSE, THE TECH NOTED THE CPR LEVER WAS ENGAGED. HE DISENGAGED THE CPR LEVER TO RESOLVE.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE HEAD OF BED WAS NOT GOING UP OR DOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1900F100

    Patients

    Seq Age Sex Outcome Treatment
    1