BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1112484 · Received August 15, 2008

    Report

    Report Number
    1824206-2008-00558
    Event Type
    Malfunction
    Date Received
    August 15, 2008
    Date of Event
    January 16, 2006
    Report Date
    January 16, 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 STATES THAT THE RH HEAD SIDERAIL WILL NOT LATCH IN THE UP POSITION. ACCOUNT STATED THAT HE HAS SPRAYED PENETRATING OIL ONTO THE PINS IN THE CENTER ARM ASSY, BUT IS STILL HAVING THE SAME PROBLEM. SUGGESTED REPLACEMENT OF THE CENTER ARM ASSY. SENDING HIM A CENTER ARM ASSY. SPOKE TO ACCOUNT, STATED THAT HE REPLACED THE CENTER ARM ASSY, AND THE PROBLEM WITH THE RH HEAD SIDERAIL NOT LATCHING HAS BEEN RESOLVED.

    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