BEUDAMED
    FDA Enforcement Class I Ongoing

    Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: HEART BASIN PACK-LF

    Recall: Z-1458-2025 · Reported April 16, 2025

    Enforcement

    Recall Number
    Z-1458-2025
    Event ID
    96443
    Classification
    Class I
    Status
    Ongoing
    Product Type
    Devices
    Firm
    MEDLINE INDUSTRIES, LP - Northfield
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    E-Mail
    Report Date
    April 16, 2025
    Initiation Date
    February 21, 2025
    Classification Date
    April 4, 2025
    Address
    3 Lakes Dr, N/A, Northfield, IL, 60093-2753, United States

    Description

    Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: HEART BASIN PACK-LF

    Reason

    Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.

    Code Info

    HEART BASIN PACK-LF, UDI/DI 10195327563561 (ea) 40195327563562 (case), Lot Numbers 24BMB798, 24DMH381, 24EMF949, 24GMF161, 24IMB237.

    Distribution

    US: CA, FL, MN, NY, OH, OR, PA, TX, WV

    Quantity

    320 units