BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA

    MDR report key: 2780911 · Received September 27, 2012

    Report

    Report Number
    2780911
    Event Type
    Malfunction
    Date Received
    September 27, 2012
    Date of Event
    September 26, 2012
    Report Date
    September 27, 2012
    Manufacturer
    HILL-ROM
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US

    Narratives

    Description of Event or Problem · 1

    THE BED LOST POWER WHILE IN USE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA BED, AC-POWERED ADJUSTABLE HOSPITAL FNL HILL-ROM 852 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *