BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTAL CARE BED

    MDR report key: 3004017 · Received February 19, 2013

    Report

    Report Number
    1824206-2013-01015
    Event Type
    Malfunction
    Date Received
    February 19, 2013
    Date of Event
    September 6, 2012
    Report Date
    September 6, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND SIGNS OF FLUID INGRESS. THE TECHNICIAN USED AN ANTIOXIDANT SPRAY ON THE SIDE RAIL ELECTRICAL CONTACTS TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THAT THE SIDE RAILS HAVE NO FUNCTIONS. NO PATIENT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    71612 TOTAL CARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1