BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ITRACK 250A

    MDR report key: 4085417 · Received August 19, 2014

    Report

    Report Number
    3005641545-2014-00002
    Event Type
    Malfunction
    Date Received
    August 19, 2014
    Date of Event
    July 24, 2014
    Report Date
    August 19, 2014
    Manufacturer
    ELLEX ISCIENCE INC.
    Product Code
    MPA
    PMA / PMN Number
    K080067
    Removal / Correction Number
    3005641545-08/11/14-001R
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    THE DEVICE WAS REMOVED FROM THE PACKAGING AND WAS FOUND TO BE MISSING A SEAL ON THE STERILE BARRIER POUCH AND THEREFORE WERE NOT STERILE. THIS DEVICE WAS DETECTED AS NOT STERILE PRIOR TO USE AND WAS NOT USED FOR SURGERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    496922 ITRACK 250A OPHTHALMIC MICROCATHETER MPA ELLEX ISCIENCE INC. ITRACK 1404-03

    Patients

    Seq Age Sex Outcome Treatment
    1 Other