BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 1952694 · Received January 4, 2011

    Report

    Report Number
    1824206-2011-00032
    Event Type
    Malfunction
    Date Received
    January 4, 2011
    Date of Event
    December 7, 2010
    Report Date
    December 7, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN RECOMMENDED THAT ACCOUNT CHECK AND ADJUSTS THE CPR CABLES AND IF IT DOES NOT RESOLVE THE ISSUE THEN REPLACE THE HEAD DRIVE. NO FURTHER INFO IS AVAILABLE ON THE REPAIR OF THIS BED AT THIS TIME.

    Description of Event or Problem · 1

    ACCOUNT ALLEGED THAT ONCE THE HEAD SECTION GETS TO CERTAIN POINT IT WILL START DRIFTING. NO INJURIES OCCURRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 3200

    Patients

    Seq Age Sex Outcome Treatment
    1