BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1110545 · Received August 14, 2008

    Report

    Report Number
    1824206-2008-00172
    Event Type
    Malfunction
    Date Received
    August 14, 2008
    Date of Event
    January 10, 2006
    Report Date
    January 10, 2006
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Removal / Correction Number
    Z-0240-2008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OR, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE REPORTER LUBRICATED THE CENTER ARM ASSY, P/N 69843S, TO RESOLVE THE PROBLEM WITH THE RH FOOT SIDERAIL NOT LATCHING IN THE UP POSITION. REPORTER DID NOT HAVE THE S/N OF THE BED.

    Description of Event or Problem · 1

    THE REPORTER STATES THAT THE RH FOOT SIDERAIL WILL NOT LATCH IN THE UP POSITION. REPORTER DID NOT HAVE THE S/N OF THE BED.

    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