BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 2031764 · Received March 21, 2011

    Report

    Report Number
    1824206-2011-01711
    Event Type
    Malfunction
    Date Received
    March 21, 2011
    Date of Event
    March 2, 2011
    Report Date
    March 2, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THAT WHILE DOING PM ON BED, COULD NOT GET A GOOD GROUND READING, IT WAS TOO HIGH. REPLACED POWER CORD TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    COMPLAINANT ALLEGED THAT THEY COULD NOT GET A GOOD GROUND READING.

    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