BEUDAMED
    FDA Adverse Event Death Summary report: N

    Saline, vascular access flush

    MDR report key: 19476306 · Received June 6, 2024

    Report

    Report Number
    1417592-2024-00634
    Event Type
    Death
    Date Received
    June 6, 2024
    Date of Event
    October 30, 2023
    Report Date
    June 6, 2024
    Manufacturer
    MEDLINE INDUSTRIES LP
    Product Code
    NGT
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    IT WAS REPORTED "MY MOM GOT LEGIONELLA BACTERIA WITH PNEUMONIA AND RESPIRATORY FAILURE THEN PASSED AWAY." NO ADDITIONAL INFORMATION WAS PROVIDED.

    Description of Event or Problem · 0

    "MY MOM GOT LEGIONELLA BACTERIA WITH PNEUMONIA AND RESPIRATORY FAILURE THEN PASSED AWAY.".

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2055517 Saline, vascular access flush NGT MEDLINE INDUSTRIES LP

    Patients

    Seq Age Sex Outcome Treatment
    1 82 YR Female Other