BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2080176 · Received April 6, 2011

    Report

    Report Number
    1824206-2011-02033
    Event Type
    Malfunction
    Date Received
    April 6, 2011
    Date of Event
    March 14, 2011
    Report Date
    March 14, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN ASKED THE ACCOUNT TO CHECK THE HI LOW AND IT WORKED FINE. TECHNICIAN HAD THE ACCOUNT CHECK THE TRENDELENBURG FUNCTION FROM BOTH THE HIGH AND LOW POSITIONS AND IT WOULD NOT WORK. TECHNICIAN SUGGESTED REPLACING THE LOGIC BOARD. NO FURTHER INFORMATION IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.

    Description of Event or Problem · 1

    ACCOUNT ALLEGED THAT THE BED WILL NOT GO INTO TRENDELENBURG. THERE WERE NO REPORTED INJURIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

    Patients

    Seq Age Sex Outcome Treatment
    1