BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EYE SURGERY STRETCHER

    MDR report key: 1760152 · Received July 12, 2010

    Report

    Report Number
    1831750-2010-01504
    Event Type
    Malfunction
    Date Received
    July 12, 2010
    Date of Event
    June 18, 2010
    Report Date
    June 18, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: TENSION ADJUSTER.

    Description of Event or Problem · 1

    IT WAS REPORTED IN (B)(4) THAT THE BRAKES WERE STUCK.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 NA