BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ENDEAVOR SPRINT RX

    MDR report key: 3933726 · Received July 15, 2014

    Report

    Report Number
    9612164-2014-00936
    Event Type
    Injury
    Date Received
    July 15, 2014
    Date of Event
    September 8, 2010
    Report Date
    June 18, 2014
    Manufacturer
    MEDTRONIC IRELAND
    Product Code
    NIQ
    PMA / PMN Number
    P060033
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    BR
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    EVALUATION, RESULTS, CONCLUSIONS: INHERENT RISK OF PROCEDURE ¿ (DISSECTION). (B)(4).

    Description of Event or Problem · 1

    DURING THE INDEX PROCEDURE, THREE ENDEAVOR SPRINT DRUG ELUTING STENTS WERE IMPLANTED; ONE IN THE RCA AND TWO IN THE CX. DURING THE IMPLANT OF THE TWO STENTS IN THE CX AN ANGIOGRAPHIC COMPLICATION OF LATERAL BRANCH STENOSIS OCCURRED. TWELVE DAYS POST THE INDEX PROCEDURE, THREE ENDEAVOR SPRINT DRUG ELUTING STENTS WERE IMPLANTED IN THE LAD, AN ANGIOGRAPHIC COMPLICATION OF DISSECTION OCCURRED DURING THE IMPLANT OF THE THIRD STENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    412556 ENDEAVOR SPRINT RX STENT, CORONARY, DRUG-ELUTING NIQ MEDTRONIC IRELAND 0000907644

    Patients

    Seq Age Sex Outcome Treatment
    1 00072 YR Hospitalization