BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TIP CLEANER,DISP,STERILE

    MDR report key: 7607124 · Received June 15, 2018

    Report

    Report Number
    1320894-2018-00139
    Event Type
    Malfunction
    Date Received
    June 15, 2018
    Report Date
    June 15, 2018
    Manufacturer
    XODUS MEDICAL, INC
    Product Code
    GEI
    PMA / PMN Number
    K874775
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THIS REPORT IS BEING FILED AS A VOLUNTARY DISTRIBUTOR REPORT. THE MANUFACTURER, XODUS MEDICAL, INC., IS RESPONSIBLE FOR PERFORMING THE EVALUATION, INVESTIGATION AND ANY REMEDIAL ACTIONS RELATED TO THIS REPORTED DEVICE ISSUE.

    Description of Event or Problem · 1

    THIS IS A VOLUNTARY DISTRIBUTOR REPORT. DURING INCOMING INSPECTION, THE DISTRIBUTOR REJECTED THIS DEVICE FOR AN INSUFFICIENT HEATSEAL. THERE WAS NO CONTACT WITH THE PATIENT AS THIS WAS FOUND DURING INCOMING INSPECTION. THIS REPORT IS BEING RAISED AS A VOLUNTARY DISTRIBUTOR REPORT ON THE BASIS OF DEVICE MALFUNCTION WITH POTENTIAL FOR INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    448933 TIP CLEANER,DISP,STERILE ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES GEI XODUS MEDICAL, INC 16JUN06A

    Patients

    Seq Age Sex Outcome Treatment
    1