BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED VERSACARE FRAME

    MDR report key: 1110563 · Received August 14, 2008

    Report

    Report Number
    1824206-2008-00173
    Event Type
    Malfunction
    Date Received
    August 14, 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
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    REPORTER SAID THAT THE RH HEAD SIDERAILS WOULD NOT LATCH. HE SAID THAT HE CLEANED THE SIDERAIL CENTER ARM ASSEMBLY AND THE BED IS WORKING FINE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE BED VERSACARE FRAME MED SURGICAL FNL HILL-ROM RITTER 3200 NA

    Patients

    Seq Age Sex Outcome Treatment
    1