BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANCE BED

    MDR report key: 2883467 · Received November 14, 2012

    Report

    Report Number
    1824206-2012-07456
    Event Type
    Malfunction
    Date Received
    November 14, 2012
    Date of Event
    October 25, 2012
    Report Date
    October 25, 2012
    Manufacturer
    HILL-ROM INC
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE LATCH GUIDE WAS STUCK CAUSING THE CARDIO PULMONARY RESUSCITATION TO NOT FUNCTION. THE TECHNICIAN RELEASED THE LATCH GUIDE AND THE CARDIO PULMONARY RESUSCITATION WILL NOW LOWER THE BED.

    Description of Event or Problem · 1

    THE TECHNICIAN ALLEGED THAT THE CARDIO PULMONARY RESUSCITATION IS NOT LOWERING THE HEAD OF THE BED. NO PT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ADVANCE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC 1130

    Patients

    Seq Age Sex Outcome Treatment
    1