BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1110925 · Received August 14, 2008

    Report

    Report Number
    1824206-2008-00178
    Event Type
    Malfunction
    Date Received
    August 14, 2008
    Date of Event
    January 18, 2006
    Report Date
    January 18, 2006
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Removal / Correction Number
    Z-0240-2008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    REPORTER HAS A BED THAT THE RIGHT FOOT SIDERAIL WILL NOT LATCH. TSR STATED SIDERAIL WILL NOT LATCH DUE TO FLUID ADHERING ITSELF TO SIDERAIL MECHANISM. LUBRICATE SIDERAIL MECHANISM WITH TEFLON LUBRICANT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1