BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIFEVEST WCD 4000 SYSTEM

    MDR report key: 3003498 · Received February 11, 2013

    Report

    Report Number
    3008642652-2013-00342
    Event Type
    Malfunction
    Date Received
    February 11, 2013
    Date of Event
    January 13, 2013
    Report Date
    February 1, 2013
    Manufacturer
    ZOLL LIFECOR CORPORATION
    Product Code
    MVK
    PMA / PMN Number
    P010030
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    DEVICE EVALUATION SUMMARY: DEVICE EVALUATION OF ELECTRODE BELT SN (B)(4) HAS BEEN COMPLETED. THE REPORTED PROBLEM (ADJUST BELT OR CHECK BELT MESSAGES, CHECK TE PAD MESSAGES) HAS BEEN CONFIRMED. AS RECEIVED, WHITE PULSE WIRE BETWEEN ECG A AND ECG B WAS OPEN. THE OPEN PULSE WIRE CAUSED THE ADJUST BELT AND CHECK TE PAD MESSAGES. THE ROOT CAUSE OF THE OPEN PULSE WIRE WAS UNABLE TO BE POSITIVELY DETERMINED. NO ADVERSE EVENT RESULTED FROM THE OPEN ELECTRODE BELT WIRE. THE PATIENT RECEIVED A REPLACEMENT ELECTRODE BELT.

    Description of Event or Problem · 1

    (B)(6) MALE PATIENT CONTACTED ZOLL CUSTOMER SUPPORT TO REPORT CHECK THERAPY ELECTRODE PAD MESSAGES AND ADJUST BELT OR CHECK BELT MESSAGES. THE PATIENT WAS ISSUED A REPLACEMENT ELECTRODE BELT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    59223 LIFEVEST WCD 4000 SYSTEM WEARABLE CARDIOVERTER DEFIBRILLATOR MVK ZOLL LIFECOR CORPORATION WCD 4000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR