BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1090524 · Received August 5, 2008

    Report

    Report Number
    1824206-2008-00712
    Event Type
    Malfunction
    Date Received
    August 5, 2008
    Date of Event
    December 13, 2005
    Report Date
    December 13, 2005
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Removal / Correction Number
    Z-0240-2008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    .

    Description of Event or Problem · 1

    THE SIDERAILS ARE NOT LATCHING ON THIS BED. TSR CLEANED AND LUBRICATED THE CENTER ARM TO RESOLVE THE ISSUE WITH THIS BED.

    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