BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 3002644 · Received February 14, 2013

    Report

    Report Number
    1824206-2013-00990
    Event Type
    Malfunction
    Date Received
    February 14, 2013
    Date of Event
    January 29, 2013
    Report Date
    January 29, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NH, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE HILL-ROM TECH FOUND THAT THE CENTER ARM ASSEMBLY WAS BROKEN. IT APPEARED THAT THE SIDERAIL HAD BEEN HIT WITH SOMETHING CAUSING THE CENTER ARM ASSEMBLY TO BREAK. PARTS HAVE BEEN ORDERED AND WILL BE REPLACED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATED THE RIGHT SIDERAIL WOULD NOT LATCH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    65289 VERSACARE BED AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

    Patients

    Seq Age Sex Outcome Treatment
    1