BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EYE SURGERY STRETCHER

    MDR report key: 1902489 · Received November 12, 2010

    Report

    Report Number
    1831750-2010-03718
    Event Type
    Malfunction
    Date Received
    November 12, 2010
    Date of Event
    October 13, 2010
    Report Date
    October 13, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    OTHER: BROKEN SIDERAILS.

    Description of Event or Problem · 1

    IT WAS REPORTED THROUGH A SERVICE REPORT THAT THE SIDERAILS WERE BROKEN. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1