BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 6102371 · Received November 15, 2016

    Report

    Report Number
    6102371
    Event Type
    Malfunction
    Date Received
    November 15, 2016
    Date of Event
    October 4, 2016
    Report Date
    October 7, 2016
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    AZ, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE SURGICAL PROCEDURE WAS COMPLETE. WHILE PATIENT BEING TRANSFERRED FROM OPERATING ROOM TABLE THAT WAS LOCKED TO THE STRETCHER, THE STRETCHER MOVED. THE PATIENT FELL TO THE GROUND BETWEEN THE OPERATING ROOM TABLE AND THE BED. STAFF SUPPORTED THE PATIENT DURING FALL. C-SPINE PRECAUTIONS PLACED. FURTHER TESTS AND MONITORING REQUIRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    754942 TRANSTAR STRETCHER STRETCHER, WHEELED FPO HILL-ROM, INC. P8000

    Patients

    Seq Age Sex Outcome Treatment
    1 19 YR Other O.R. TABLE-LOCKED