BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRAUMA STRETCHER

    MDR report key: 1972455 · Received December 30, 2010

    Report

    Report Number
    1831750-2010-05428
    Event Type
    Malfunction
    Date Received
    December 30, 2010
    Date of Event
    December 6, 2010
    Report Date
    December 6, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE STRETCHER WAS NOT WORKING PROPERLY. THE BACKREST WOULD NOT GO DOWN TO THE FULLY DOWN POSITION. IT WAS ALSO REPORTED THE FOOT END JACK DRIFTED DOWN. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE ARE ADVERSE CONSEQUENCES TO REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRAUMA STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIV. 1020 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK