BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COMBISET WITH BVM

    MDR report key: 1922588 · Received November 19, 2010

    Report

    Report Number
    8030665-2010-00073
    Event Type
    Malfunction
    Date Received
    November 19, 2010
    Date of Event
    November 12, 2010
    Report Date
    November 19, 2010
    Manufacturer
    REYNOSA MANUFACTURING
    Product Code
    FJK
    PMA / PMN Number
    K962081
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    NO INFORMATION

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE MANUFACTURER IS REVIEWING THE DESIGN HISTORY FILE AND THE LOT AND MANUFACTURING RECORDS FOR THIS PRODUCT. IN ADDITION, THE MANUFACTURER HAS MADE VISITS TO THESE CLINICS TO OBSERVE THE CLINICAL PRACTICE AND COLLECT INFORMATION THAT WILL BE HELPFUL TO THE INVESTIGATION. THE INVESTIGATION IS ONGOING AND A ROOT CAUSE HAS NOT YET BEEN DETERMINED AT THIS TIME.

    Description of Event or Problem · 1

    A REPORT HAS BEEN REC'D FROM (B)(6) OF A POSSIBLE BLOODLINE TUBING KINK ON THE ARTERIAL LINE OF THE BVM COMBISET BLOODLINE. REPORTEDLY, THE INCIDENT OCCURRED WHILE THE PT WAS RECEIVING HEMODIALYSIS TREATMENT WHEN THE NURSE NOTICED THAT THE ARTERIAL LINE WAS KINKED AT THE BVM INLET. ALTHOUGH, THERE WAS PT INVOLVEMENT, THERE WAS NO INJURY TO THE PT AND NO MEDICAL INTERVENTION REQUIRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COMBISET WITH BVM DIALYSIS BLOODLINE TUBING FJK REYNOSA MANUFACTURING NA 10JR01040

    Patients

    Seq Age Sex Outcome Treatment
    1 NA