BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2100205 · Received May 16, 2011

    Report

    Report Number
    1824206-2011-02727
    Event Type
    Malfunction
    Date Received
    May 16, 2011
    Date of Event
    April 15, 2011
    Report Date
    April 25, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ON (B)(6) 2011 AT 10:32 AM IN THE OPERATING ROOM, THEY TRANSPORTED THE PT FROM A TABLE TO THE STRETCHER AND ALLEGED THE STRETCHER MOVED WHEN THEY WENT TO PLACE THE PT ON IT. THE PT FELL TO THE FLOOR AND NO INJURIES WERE REPORTED FROM THIS FALL. THE ACCOUNT DID NOT SPECIFY IF THE CASTERS ROLLED, SWIVELED OR SLID. THE DOCTOR SAID THE BRAKES WERE SET. THE ACCOUNT TOOK THE STRETCHER OUT OF SERVICE AND CONFIRMED THAT THE BRAKES WORKED PROPERLY. CURRENTLY THE STRETCHER IS LOCKED IN A ROOM, OUT OF SERVICE. THE ACCOUNT WILL NOT ALLOW THE FIELD TECHNICIAN TO INSPECT THE STRETCHER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM INC. 8000

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK