BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 3071035 · Received April 8, 2013

    Report

    Report Number
    1824206-2013-02000
    Event Type
    Malfunction
    Date Received
    April 8, 2013
    Date of Event
    March 12, 2013
    Report Date
    March 12, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE HEAD DRIVE WAS FOUND TO BE DEFECTIVE. HILL-ROM HAS ATTEMPTED TO F/U WITH THE CUSTOMER TO ENSURE RESOLUTION. HOWEVER, NO OTHER INFO HAS BEEN OBTAINED AT THIS TIME.

    Description of Event or Problem · 1

    CUSTOMER ALLEGES THE HEAD SECTION WILL NOT LOWER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    144294 VERSACARE BED AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

    Patients

    Seq Age Sex Outcome Treatment
    1