BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EYE SURGERY STRETCHER

    MDR report key: 2133824 · Received May 12, 2011

    Report

    Report Number
    1831750-2011-04585
    Event Type
    Malfunction
    Date Received
    May 12, 2011
    Date of Event
    April 14, 2011
    Report Date
    April 14, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT UPON INITIAL INSPECTION, THE STRETCHER DOES NOT MOVE AS THE AXLES ARE NOT WORKING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    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