BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 2920797 · Received December 26, 2012

    Report

    Report Number
    1824206-2012-08562
    Event Type
    Malfunction
    Date Received
    December 26, 2012
    Date of Event
    December 10, 2012
    Report Date
    December 10, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN ISOLATED THE DRIFT TO HEAD UP VALVE. HE FOUND THAT THE HEAD UP VALVE WAS WORN FROM AGE. HE REPLACED THE HEAD UP VALVE AND THE BED FUNCTIONED TO SPECIFICATIONS.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THAT THE HEAD OF THE BED WAS DRIFTING DOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1