BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 1851994 · Received September 24, 2010

    Report

    Report Number
    1824206-2010-10113
    Event Type
    Malfunction
    Date Received
    September 24, 2010
    Date of Event
    August 30, 2010
    Report Date
    August 30, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND WATER FILTRATION ON THE POWER CONTROL BOARD. TECHNICIAN REPLACED THE POWER CONTROL BOARD AND THE POWER IS RESTORED.

    Description of Event or Problem · 1

    TECHNICIAN ALLEGED THAT THE BED HAS NO POWER. NO PATIENT IMPACT REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P1050

    Patients

    Seq Age Sex Outcome Treatment
    1