BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CARDIOVASCULAR PROCEDURE KIT

    MDR report key: 1894757 · Received November 5, 2010

    Report

    Report Number
    1212122-2010-00202
    Event Type
    Malfunction
    Date Received
    November 5, 2010
    Date of Event
    October 21, 2010
    Report Date
    October 21, 2010
    Manufacturer
    TERUMO CARDIOVASCULAR SYSTEMS CORPORATION
    Product Code
    OEZ
    PMA / PMN Number
    EXEMPT
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TERUMO DID NOT RECEIVE THE ACTUAL DEVICE; HOWEVER, PHOTOS WERE RECEIVED CONFIRMING THE KINK IN TUBING AT THE Y CONNECTOR. THE ROOT CAUSE OF THIS EVENT IS DUE TO LAYERING AND LINE PLACEMENT ON THE Y CONNECTOR. THE COMPLAINT WAS MISREPORTED; THE EVENT OCCURRED OUT-OF-BOX. THERE HAVE BEEN REPORTS OF KINKED TUBING IN OTHER PACKS. LAYERING HAS BEEN REVISED TO AVOID FUTURE KINKING IN PACKS. THE COMPLAINT WILL BE INCLUDED IN ASSOCIATE AWARENESS TRAINING. THE DEVICE HISTORY RECORD DID NOT INDICATE ANY PRODUCTION RELATED PROBLEMS. ALL AVAILABLE INFO HAS BEEN PLACED IN FILE IN QUALITY MANAGEMENT FOR APPROPRIATE TRACKING, TRENDING, AND FOLLOW UP. (B)(4).

    Description of Event or Problem · 1

    THE USER FACILITY REPORTED TO TERUMO CARDIOVASCULAR THAT DURING CARDIOPULMONARY BYPASS SURGERY, THERE WAS A KINK IN TUBING. THE CUSTOMER HAS REPORTED THAT THIS IS AN ONGOING PROBLEM. THE PRODUCT WAS NOT CHANGED OUT, THERE WAS NO BLOOD LOSS, AND SURGERY WAS COMPLETED SUCCESSFULLY. THE EVENT DID NOT CAUSE DELAY IN SURGICAL PROCEDURE. THERE WAS NO HARM TO THE PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CARDIOVASCULAR PROCEDURE KIT CONVENIENCE TUBING PACK OEZ TERUMO CARDIOVASCULAR SYSTEMS CORPORATION NA MK09

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK