BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EYE SURGERY STRETCHER

    MDR report key: 2031553 · Received March 21, 2011

    Report

    Report Number
    1831750-2011-02629
    Event Type
    Malfunction
    Date Received
    March 21, 2011
    Date of Event
    February 14, 2011
    Report Date
    February 22, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    THE BIOMEDICAL DEPARTMENT OF THE HOSPITAL REPORTED THAT "THE CART CANNOT STAY IN HIGH POSITION". THERE WERE NO ADVERSE CONSEQUENCES FOR PTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EYE SURGERY STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1089 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA