BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ELECTRIC STRETCHER

    MDR report key: 2050680 · Received March 14, 2011

    Report

    Report Number
    1831750-2011-02461
    Event Type
    Malfunction
    Date Received
    March 14, 2011
    Date of Event
    February 15, 2011
    Report Date
    February 15, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE ELECTRIC STRETCHER NEEDS REPAIR. THE FOOT END JACK WILL NOT GO ALL OF THE WAY UP. IT IS UNKNOWN IF THERE WAS PATIENT 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 INK STRYKER MEDICAL 1550 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK