BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2080178 · Received April 6, 2011

    Report

    Report Number
    1824206-2011-02034
    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
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT INSPECTED THE CPR CABLES AND HANDLES AND THEY WERE IN PROPER WORKING ORDER. TECHNICIAN SUGGESTED THAT THE ACCOUNT REPLACE THE HEAD DRIVE MOTOR. NO FURTHER INFORMATION ON THE REPAIR OF THE BED IS AVAILABLE AT THIS TIME.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THAT THE HEAD SECTION DRIFTED DOWN ON THIS BED. THE ACCOUNT STATED THAT THERE WERE NO 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