BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 2831492 · Received October 11, 2012

    Report

    Report Number
    1824206-2012-06415
    Event Type
    Malfunction
    Date Received
    October 11, 2012
    Date of Event
    September 24, 2012
    Report Date
    September 25, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE HILL-ROM TECHNICIAN REPORTED THAT THE TICKING WAS WORN DUE TO AGE AND HAD SOME SMALL PINS HOLES IN THE COVER RESULTING IN VISIBLE STAINS ON THE TOPPER FOAM. HE INSTALLED A TICKING KIT TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATED FLUID INGRESS WAS FOUND IN THE MATTRESS.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1