BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1112464 · Received August 15, 2008

    Report

    Report Number
    1824206-2008-00556
    Event Type
    Malfunction
    Date Received
    August 15, 2008
    Date of Event
    November 14, 2005
    Report Date
    November 14, 2005
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Removal / Correction Number
    Z-0240-2008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ACCOUNT CALLED AND ALLEGED THAT ONE OF HIS SIDERAILS WOULD NOT LATCH. HE SAID THAT THE PINS ARE NOT RELEASING TO LOCK IT INTO PLACE. ACCOUNT WAS INSTRUCTED TO CLEAN THE D-PINS AND LUBRICATE THEM SLIGHTLY. ACCOUNT CLEANED AND RELUBRICATED THE SIDERAIL LATCH PINS, AND THIS RESOLVED THE ISSUE.

    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