BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 2760170 · Received September 20, 2012

    Report

    Report Number
    1824206-2012-05689
    Event Type
    Malfunction
    Date Received
    September 20, 2012
    Date of Event
    August 29, 2012
    Report Date
    August 29, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN REPLACED THE CARDIO PULMONARY RESUSCITATION VALVE AND THE HEAD DOWN VALVE TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE TECHNICIAN ALLEGED THAT THE HEAD OF BED WILL NOT LOWER BY THE CARDIO PULMONARY RESUSCITATION LEVEL OR THE SIDE RAIL CONTROLS. NO PATIENT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1