BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1151144 · Received September 9, 2008

    Report

    Report Number
    1824206-2008-01535
    Event Type
    Malfunction
    Date Received
    September 9, 2008
    Date of Event
    December 22, 2006
    Report Date
    December 22, 2006
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Removal / Correction Number
    Z-0240-2008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ACCOUNT ALLEGES THAT SIDERAIL WILL NOT LATCH. INSTALLED LATECH KIT AND IT RESOLVED ISSUE. 140865.

    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