BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NATURALYTE

    MDR report key: 3935950 · Received June 23, 2014

    Report

    Report Number
    1225714-2014-05067
    Event Type
    Injury
    Date Received
    June 23, 2014
    Date of Event
    June 19, 2008
    Report Date
    May 23, 2014
    Manufacturer
    FRESENIUS MEDICAL CARE NORTH AMERICA
    Product Code
    KPO
    PMA / PMN Number
    K070177
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Additional Manufacturer Narrative · 1

    THIS IS ONE OF THREE EVENTS (CARDIOVASCULAR) FOR THE SAME PATIENT INVOLVING THREE SEPARATE PRODUCTS; ASSOCIATED MDR 1225714-2014-05066, 1225714-2014-05067, 1225714-2014-05068, 1225714-2014-05069, 1225714-2014-05070, 1225714-2014-05071, 2937457-2014-01176, 2937457-2014-01177 AND 2937457-2014-01178.

    Description of Event or Problem · 1

    THE PLAINTIFF'S ATTORNEY ALLEGED THAT THE PLAINTIFF EXPERIENCED CARDIOVASCULAR EVENTS ON OR ABOUT (B)(6) 2008, (B)(6) 2008 AND 07/2013 AFTER THE USE OF THE PRODUCT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    366834 NATURALYTE NONE KPO FRESENIUS MEDICAL CARE NORTH AMERICA

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| L| O| R| S