BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2800336 · Received October 9, 2012

    Report

    Report Number
    1824206-2012-06254
    Event Type
    Malfunction
    Date Received
    October 9, 2012
    Date of Event
    September 19, 2012
    Report Date
    September 19, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN ISOLATED THE ISSUE TO A WORN POWER CORD PLUG. HE REPLACED THE POWER CORD PLUG TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES DURING A PREVENTIVE MAINTENANCE CHECK, THE TECHNICIAN FOUND THAT THE GROUND RESISTANCE READING WAS OUT OF NORMAL RANGE.

    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