BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ST104 TRANSPORT OBS

    MDR report key: 2221874 · Received July 21, 2011

    Report

    Report Number
    1831750-2011-07471
    Event Type
    Malfunction
    Date Received
    July 21, 2011
    Date of Event
    June 23, 2011
    Report Date
    June 23, 2011
    Manufacturer
    STRYKER MEDICAL
    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 HEAD END OF THE STRETCHER WAS DRIFTING DOWN. THE CUSTOMER COULD NOT DETERMINE WHETHER THERE WAS PT INVOLVEMENT, HOWEVER, NO ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ST104 TRANSPORT OBS WHEELED STRETCHER FPO STRYKER MEDICAL 0735 NA

    Patients

    Seq Age Sex Outcome Treatment
    1