BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1093724 · Received August 5, 2008

    Report

    Report Number
    1824206-2008-00605
    Event Type
    Malfunction
    Date Received
    August 5, 2008
    Date of Event
    September 7, 2005
    Report Date
    September 7, 2005
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Removal / Correction Number
    Z-0240-2008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    TECH SAID THE RH HEAD SIDERAIL WAS NOT LATCHING. TECH CLEANED AND LUBRICATED PART NUMBER 69843S SIDERAIL CENTER AND THE BED IS WORKING FINE.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1