BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2012070 · Received February 14, 2011

    Report

    Report Number
    1824206-2011-00847
    Event Type
    Malfunction
    Date Received
    February 14, 2011
    Date of Event
    January 21, 2011
    Report Date
    January 21, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH REPLACED THE POWER CORD TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE TECH FOUND THE BED WAS GIVING THE PROPER READINGS FOR GROUND RESISTANCE. HE FOUND THE GROUND PIN WAS LOOSE ON THE POWER CORD PLUG.

    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