BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PRIME ZOOM STRETCHER, 30" LITTER

    MDR report key: 2223326 · Received August 15, 2011

    Report

    Report Number
    1831750-2011-08679
    Event Type
    Malfunction
    Date Received
    August 15, 2011
    Date of Event
    July 19, 2011
    Report Date
    July 19, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    PMA / PMN Number
    K022309
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END OF THE STRETCHER WAS NOT RISING. THE CUSTOMER COULD NOT DETERMINE WHETHER THERE WAS PT INVOLVEMENT OR ADVERSE CONSEQUENCES OCCURRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRIME ZOOM STRETCHER, 30" LITTER WHEELED POWERED STRETCHER FNL STRYKER MEDICAL 1125000030 NA

    Patients

    Seq Age Sex Outcome Treatment
    1