BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 3223855 · Received July 2, 2013

    Report

    Report Number
    1824206-2013-03319
    Event Type
    Malfunction
    Date Received
    July 2, 2013
    Date of Event
    June 6, 2013
    Report Date
    June 3, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WV, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE SIDE RAIL HEAD DOWN MEMBRANE SWITCH IS SHORTED OUT. THE TECHNICIAN REPLACED THE SIDE RAIL HEAD DOWN MEMBRANE SWITCH TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE TECHNICIAN ALLEGED THE HEAD OF THE BED IS LOWERING ON ITS OWN. NO PATIENT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    301498 CENTRA BED A/C POWERED ADJUSTABLE HOSP. BED FNL HILL-ROM, INC. 850

    Patients

    Seq Age Sex Outcome Treatment
    1