BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EYE SURGERY STRETCHER

    MDR report key: 2864742 · Received November 8, 2012

    Report

    Report Number
    1831750-2012-11724
    Event Type
    Malfunction
    Date Received
    November 8, 2012
    Date of Event
    October 11, 2012
    Report Date
    October 11, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS - RELEASE ROD.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE JACK WAS DRIFTING DUE TO A WORN SPRING ON THE RELEASE ROD. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EYE SURGERY STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1069 NA

    Patients

    Seq Age Sex Outcome Treatment
    1