BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ELECTRIC STRETCHER

    MDR report key: 2022015 · Received March 10, 2011

    Report

    Report Number
    1831750-2011-02363
    Event Type
    Malfunction
    Date Received
    March 10, 2011
    Date of Event
    February 10, 2011
    Report Date
    February 10, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE OPERATION MANUAL FOR THIS STRETCHER CONTAINS THE FOLLOWING INSTRUCTIONS, "THE FOWLER AND/OR KNEE GATCH MUST BE RESET AFTER THE EMERGENCY DROP FEATURE IS USED OR THEY WILL NOT RAISE. TO RESET, PRESS AND HOLD THE PT CONTROL FOWLER AND KNEE GATCH DOWN BUTTONS UNTIL THE MOTOR STOPS. FOR FASTER RESET, MANUALLY LIFT FOWLER AND KNEE GATCH UNTIL LOCKED."

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE HEAD END OF THE BED IS NOT WORKING PROPERLY. THE FOWLER WOULD NOT RAISE UP. 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 ELECTRIC STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1550 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK