BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TENDRIL ST

    MDR report key: 3923232 · Received July 9, 2014

    Report

    Report Number
    2017865-2014-14544
    Event Type
    Injury
    Date Received
    July 9, 2014
    Date of Event
    April 14, 2014
    Manufacturer
    ST. JUDE MEDICAL, INC., CRMD
    Product Code
    NVN
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    ALL INFORMATION PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT CHEST X-RAY CONFIRMED THE RIGHT ATRIAL LEAD HAD DISLODGED. THE LEAD WAS CAPPED AND REPLACED ON (B)(6) 2014. THE PATIENT EXPERIENCED AN UNSPECIFIED HAEMODYNAMIC ISSUE DURING THE REVISION PROCEDURE. AS A PRECAUTION THE PATIENT WAS PLACED IN THE INTENSIVE CARE UNIT AND THE CONDITION WAS STABILIZED. PATIENT WAS IN GOOD CONDITION AND DISCHARGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    401616 TENDRIL ST PERMANENT PACEMAKER ELECTRODE NVN ST. JUDE MEDICAL, INC., CRMD 1788TC/52 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention (B)(4), (B)(4)