BEUDAMED
    FDA Adverse Event Death Summary report: N

    LUMAX 740 DR-T

    MDR report key: 3173918 · Received June 17, 2013

    Report

    Report Number
    1028232-2013-01676
    Event Type
    Death
    Date Received
    June 17, 2013
    Date of Event
    May 29, 2013
    Report Date
    June 5, 2013
    Manufacturer
    BIOTRONIK SE & CO. KG
    Product Code
    MRM
    PMA / PMN Number
    P000009
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OR, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE WAS NOT RETURNED FOR ANALYSIS. THE ANALYSIS IS THEREFORE BASED ON THE INSPECTION OF THE QUALITY DOCUMENTS ASSOCIATED WITH THE MANUFACTURE OF THIS PARTICULAR DEVICE. THE MANUFACTURING PROCESS FOR THIS DEVICE WAS RE-INVESTIGATED. ALL PRODUCTION STEPS HAD BEEN PERFORMED ACCORDINGLY. THERE WAS NO SIGN OF ANY INCONSISTENCY DURING THE MANUFACTURING PROCESS WHICH MIGHT BE RELATED TO THE CLINICAL OBSERVATION. IN SUMMARY, THE DEVICE WAS NOT RETURNED FOR ANALYSIS. THE REVIEW OF THE QUALITY DOCUMENTS CONFIRMED A REGULAR DEVICE MANUFACTURING.

    Description of Event or Problem · 1

    PER PATIENT'S WIFE, THIS PATIENT RECEIVED MULTIPLE SHOCKS AND EXPIRED THE SAME DAY. THE CAUSE OF DEATH IS UNKNOWN. IT IS UNKNOWN IF THIS DEVICE WILL BE RETURNED FOR ANALYSIS. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, THIS FILE WILL BE UPDATED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    273011 LUMAX 740 DR-T ICD MRM BIOTRONIK SE & CO. KG 365606

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Death