BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UNKNOWN STRETCHER MODEL

    MDR report key: 2033322 · Received March 22, 2011

    Report

    Report Number
    1831750-2011-02645
    Event Type
    Malfunction
    Date Received
    March 22, 2011
    Date of Event
    February 28, 2011
    Report Date
    February 28, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY THE SERVICE REPORT THAT THE STRETCHER TIPPED (FOOT END CASTERS LEFT THE GROUND). THE PT WAS SITTING MIDWAY BETWEEN THE HEAD OF THE STRETCHER AND THE CENTER OF THE STRETCHER. THE PT WENT TO MOVE FROM A SITTING POSITION TO RECLINED POSITION BUT RECLINED WITH HIS HEAD AND NECK HANGING OFF OF THE HEAD END OF THE STRETCHER. THE PT WAS A VERY LARGE PERSON. THE PT FELL BUT NO INJURY OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNKNOWN STRETCHER MODEL HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 5050 NA

    Patients

    Seq Age Sex Outcome Treatment
    1