BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2050850 · Received April 4, 2011

    Report

    Report Number
    1824206-2011-01990
    Event Type
    Malfunction
    Date Received
    April 4, 2011
    Date of Event
    March 16, 2011
    Report Date
    March 16, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND BED IN "DOWN" STORAGE. NO PATIENT IMPACT REPORTED. COMPLAINT: HEAD UP FUNCTION NOT WORKING. FUNCTION DOES NOT WORK MANUALLY OR UNDER POWER. BATTERY LED IS ON. CAUSE: FAULTY VALVE GUIDE TUBE. REPLACED HEAD UP VALVE GUIDE TUBE TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    INFORMATION PROVIDED ALLEGED THAT THE HEAD UP FUNCTION WAS NOT WORKING. FUNCTION DOES NOT WORK MANUALLY OR UNDER POWER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1900

    Patients

    Seq Age Sex Outcome Treatment
    1