BEUDAMED
    FDA Adverse Event Other Summary report: N

    VERSACARE

    MDR report key: 1736312 · Received June 22, 2010

    Report

    Report Number
    1824206-2010-08399
    Event Type
    Other
    Date Received
    June 22, 2010
    Date of Event
    May 25, 2010
    Report Date
    May 25, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN COULD NOT DUPLICATE THE HI/LOW FUNCTION LOCKING OUT.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THAT THE BED HI/LOW FUNCTION WAS LOCKED OUT DURING A PT CODE. THE ACCOUNT WOULD NOT RELEASE ANY INFORMATION REGARDING THE INCIDENT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK