BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIFEVEST WCD 3000 SYSTEM

    MDR report key: 1210126 · Received October 20, 2008

    Report

    Report Number
    3002158293-2008-00550
    Event Type
    Malfunction
    Date Received
    October 20, 2008
    Date of Event
    October 1, 2008
    Report Date
    October 17, 2008
    Manufacturer
    ZOLL LIFECOR CORPORATION
    Product Code
    MVK
    PMA / PMN Number
    P010030
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    DEVICE EVALUATION SUMMARY: DEVICE EVALUATION OF BATTERY PACK HAS BEEN COMPLETED. THE REPORTED PROBLEM WAS CONFIRMED. THE CAUSE OF THE BATTERY PACK NOT CHARGING WAS WATER WITHIN THE BATTERY PACK. THE ROOT CAUSE OF THE WATER IS NOT KNOWN, BUT IS PROBABLY DUE TO THE PT SUBMERSING THE BATTERY PACK IN WATER. THE BATTERY PACK WAS SCRAPPED. NO ADVERSE EVENT RESULTED FROM THE FAULTY BATTERY PACK. THE LAST PT TO USE THIS BATTERY PACK DID NOT REPORT ANY PROBLEMS.

    Description of Event or Problem · 1

    A REVIEW OF SERVICE DATA DETECTED A REPORTABLE EVENT. DURING SERVICING OF BATTERY PACK WHICH WAS RETURNED FOR ROUTINE MAINTENANCE, IT WAS DISCOVERED THAT THE BATTERY PACK WOULD NOT CHARGE. THE LAST PATIENT TO USE THIS BATTERY PACK DID NOT REPORT ANY PROBLEMS WITH IT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIFEVEST WCD 3000 SYSTEM WEARABLE CARDIOVERTER DEFIBRILLATOR MVK ZOLL LIFECOR CORPORATION WCD 3000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA