BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1111980 · Received August 15, 2008

    Report

    Report Number
    1824206-2008-00371
    Event Type
    Malfunction
    Date Received
    August 15, 2008
    Date of Event
    July 5, 2006
    Report Date
    July 5, 2006
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Removal / Correction Number
    Z-0240-2008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    REPORTER SAID THAT THE ACCOUNT HAS TWO BEDS THAT SIDERAIL WOULD NOT LATCH AND THE ONE BED HAS A SOLID WRENCH LED ON. HE NEEDS A WARRANTY WORK ORDER FOR THESE BEDS. REPORTER SAID THAT HE NEEDED A CAREGIVER BOARD AND SCREW COVERS SHIPPED TO THE ATTENTION OF MAINTENANCE. TSR INSTALLED SIDERAIL INLINE KIT AND THE BED IS WORKING FINE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 3200

    Patients

    Seq Age Sex Outcome Treatment
    1