BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GRANUFLO

    MDR report key: 3874952 · Received June 2, 2014

    Report

    Report Number
    1225714-2014-03724
    Event Type
    Injury
    Date Received
    June 2, 2014
    Date of Event
    May 1, 2007
    Report Date
    April 30, 2014
    Manufacturer
    FRESENIUS MEDICAL CARE NORTH AMERICA
    Product Code
    KPO
    PMA / PMN Number
    K030497
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Additional Manufacturer Narrative · 1

    THIS IS ONE EVENT FOR THE SAME PATIENT INVOLVING TWO SEPARATE PRODUCTS; ASSOCIATED MDR #1225714-2014-03724 AND 1225714-2014-03725.

    Description of Event or Problem · 1

    THE PLAINTIFF'S ATTORNEY ALLEGED THA THE PATIENT EXPERIENCED A CARDIOVASCULAR EVENT IN (B)(6) 2007, AFTER THE USE OF THE PRODUCT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    320955 GRANUFLO KPO FRESENIUS MEDICAL CARE NORTH AMERICA

    Patients

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