BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2151400 · Received June 8, 2011

    Report

    Report Number
    1824206-2011-03145
    Event Type
    Malfunction
    Date Received
    June 8, 2011
    Date of Event
    May 18, 2011
    Report Date
    May 18, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE BIOMED REPLACED THE CAREGIVER CIRCUIT BOARD TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE BIOMED STATED THE BED IS LOCKED OUT AND FLASHING ERROR 4. WHEN HE OPENED THE SIDERAIL HE FOUND FLUID ON THE CAREGIVER CIRCUIT BOARD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

    Patients

    Seq Age Sex Outcome Treatment
    1