BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1151723 · Received September 10, 2008

    Report

    Report Number
    1824206-2008-01665
    Event Type
    Malfunction
    Date Received
    September 10, 2008
    Date of Event
    April 26, 2007
    Report Date
    April 26, 2007
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Removal / Correction Number
    Z-0240-2008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ACCOUNT HAS A BED THAT THE SIDERAILS WILL NOT LATCH. ACCOUNT INSTALLED TO SIDERAIL LATCH KIT (140865) 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