BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA 850 BED

    MDR report key: 2253854 · Received August 11, 2011

    Report

    Report Number
    1824206-2011-04254
    Event Type
    Malfunction
    Date Received
    August 11, 2011
    Date of Event
    August 1, 2011
    Report Date
    August 1, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND HIGH GROUND READING IN AC PLUG - GROUND PIN WAS BROKEN. REPLACED THE BROKEN PLUG TO RESOLVE THIS ISSUE. BED LOCATED IN STORAGE.

    Description of Event or Problem · 1

    COMPLAINT OF BED NOT WORKING. BED IN STORAGE AREA. NO INJURY ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA 850 BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P850

    Patients

    Seq Age Sex Outcome Treatment
    1