BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1110705 · Received August 14, 2008

    Report

    Report Number
    1824206-2008-00148
    Event Type
    Malfunction
    Date Received
    August 14, 2008
    Date of Event
    May 24, 2005
    Report Date
    May 24, 2005
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Removal / Correction Number
    Z-0240-2008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECH WAS QUESTIONED BY ACCOUNT IF THERE WAS ANYTHING THEY CAN DO. TECH TOLD ACCOUNT THERE IS NOTHING AT THIS TIME AND ENG SAYS THERE ISW NO NEED FOR LUBRICATION AND THOUGHT THAT FIELD TECH'S MIGHT BE USI8NG A TEFLON LUBRICANT. NO PROBLEMS AT THIS TIME.

    Description of Event or Problem · 1

    HILL-ROM WAS PERFORMING AN INSERVICING AND IT COME UP THAT THEY ARE HAVING CONTINUING PROBLEMS WITH SIDERAILS LATCHING.

    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