BEUDAMED
    FDA Adverse Event Death Summary report: N

    FLEXIFLO ENTERAL FEEDING TUBE

    MDR report key: 310506 · Received December 22, 2000

    Report

    Report Number
    1528738-2000-00064
    Event Type
    Death
    Date Received
    December 22, 2000
    Date of Event
    October 1, 2000
    Report Date
    November 22, 2000
    Manufacturer
    ROSS PRODUCTS DIVISION / ABBOTT LABORATORIES
    Product Code
    BSS
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    PHYSICIAN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FLEXIFLO ENTERAL FEEDING TUBE 78 BSS TUBE, NASOGASTRIC BSS ROSS PRODUCTS DIVISION / ABBOTT LABORATORIES 475 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO Death