BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2140348 · Received June 16, 2011

    Report

    Report Number
    1824206-2011-03282
    Event Type
    Malfunction
    Date Received
    June 16, 2011
    Date of Event
    June 6, 2011
    Report Date
    June 6, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECH FOUND THAT THE STRETCHER BRAKES WERE NOT FUNCTIONING ON THE FOOT SECTION. FOUND: BED BRAKE LINKAGE IS NOT ATTACHED. INSTALLED NEW BRAKE LINKAGE UPGRADE FOR THE STRETCHER TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    FACILITY ALLEGES THE STRETCHER BRAKES WERE NOT FUNCTIONING ON THE FOOT SECTION. NO ALLEGED INJURIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM INC. P8000

    Patients

    Seq Age Sex Outcome Treatment
    1