BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ENRHYTHM DR

    MDR report key: 1926513 · Received December 14, 2010

    Report

    Report Number
    6000144-2010-06431
    Event Type
    Malfunction
    Date Received
    December 14, 2010
    Date of Event
    October 6, 2010
    Manufacturer
    MEDTRONIC MED REL, INC.
    Product Code
    DXY
    PMA / PMN Number
    P980035/S38
    Removal / Correction Number
    Z-1440-2010
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. EVALUATION SUMMARY: (B)(4) THE ACTUAL DEVICE WAS NOT RECEIVED FOR EVALUATION. WE DID RECEIVE PERFORMANCE DATA COLLECTED FROM THE DEVICE AND HAVE ANALYZED THE DATA. ANALYSIS REVEALED A LOW TELEMETERED BATTERY VOLTAGE. ON (B)(4) 2010, THE TELEMETERED BATTERY VOLTAGE WAS 2.79 V, WHILE THE DAILY BATTERY VOLTAGE TREND MEASUREMENT WAS 2.93 V.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE CALLER REQUESTED A LONGEVITY ESTIMATE. THE DEVICE WAS NOTED TO HAVE A LOW TELEMETERED BATTERY VOLTAGE WHEN COMPARED TO THE SAVE TO DISK VOLTAGE. THE DEVICE IS STILL IN USE. NO PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ENRHYTHM DR IMPLANTABLE PULSE GENERATOR DXY MEDTRONIC MED REL, INC. P1501DR ASKU

    Patients

    Seq Age Sex Outcome Treatment
    1 27 YR Other 4068 (X2) IMPLANTABLE PACING LEAD