BEUDAMED
    FDA Adverse Event Death Summary report: N

    MEDLINE SALINE

    MDR report key: 18325195 · Received December 13, 2023

    Report

    Report Number
    MW5149229
    Event Type
    Death
    Date Received
    December 13, 2023
    Date of Event
    October 3, 2022
    Report Date
    December 11, 2023
    Manufacturer
    MEDLINE INDUSTRIES, LP - NORTHFIELD
    Product Code
    NGT
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    MY MOTHER (B)(6) PASSED AWAY ON (B)(6) 2022 FROM THE UNSTERILE MEDLINE SALINE PRODUCTS USED FOR MONTHS LEADING UP TO HER DEATH RECALLED FROM THE NURSE ASSIST REPORT ON (B)(6) 2023. HAD ALL THE LIFE THREATENING AFFECTS ASSOCIATED WITH THE REPORT. THANKS, (B)(6).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    273522 MEDLINE SALINE SALINE, VASCULAR ACCESS FLUSH NGT MEDLINE INDUSTRIES, LP - NORTHFIELD 22073679

    Patients

    Seq Age Sex Outcome Treatment
    1 82 YR Female Death