BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1111492 · Received August 14, 2008

    Report

    Report Number
    1824206-2008-00355
    Event Type
    Malfunction
    Date Received
    August 14, 2008
    Date of Event
    March 27, 2007
    Report Date
    March 27, 2007
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Removal / Correction Number
    Z-0240-2008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    SUM - RIGHT INTERMEDIATE SIDERAIL NOT LATCHING PROPERLY. NO ACCIDENT REPORTED. BED WAS PUT OUT OF SERVICE TO AVOID ANDY PT CONTACT. INSTALLED NEW INLINE SPRING KIT ON ALL 4 SIDERAIL TO FIX. BED PASSED THE FUNCTION TEST.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE AC POWERED HOSPITAL BED FNL HILL-ROM RITTER P3200

    Patients

    Seq Age Sex Outcome Treatment
    1