BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 2220477 · Received July 18, 2011

    Report

    Report Number
    1824206-2011-03786
    Event Type
    Malfunction
    Date Received
    July 18, 2011
    Date of Event
    June 30, 2011
    Report Date
    June 30, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OR, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN ALLEGED THAT THE NURSE CALL FUNCTION WAS NOT WORKING ON THIS BED. THE BED WAS BEING USED IN A MED SURG UNIT. TECHNICIAN SUGGESTED THAT THEY ISOLATE THE PENDANT FOR REPLACEMENT. REPAIR NOT YET COMPLETE.

    Description of Event or Problem · 1

    COMPLAINT ALLEGED THAT THE NURSE CALL FUNCTION WAS NOT WORKING ON THIS BED. NO REPORTED INJURIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P3200

    Patients

    Seq Age Sex Outcome Treatment
    1