BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE-

    MDR report key: 2161089 · Received July 5, 2011

    Report

    Report Number
    1824206-2011-03561
    Event Type
    Malfunction
    Date Received
    July 5, 2011
    Date of Event
    June 20, 2011
    Report Date
    June 20, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECH FOUND THE BED LOCATED IN HALLWAY AND TRANSPORTED IT TO BED SHOP. FOUND: HEAD HI/LOW DRIFTING. RESOLUTION: REPLACED CPR VALVE TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    COMPLAINT INFO ALLEGED THAT THE HEAD HI/LOW DRIFTING ON THIS BED. NO INJURY ALLEGED.

    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