BEUDAMED
    FDA Enforcement Class II Ongoing

    Surgical convenience kits labeled as: MEDLINE PLASTICS/PEDS KIT, Reorder Number DYNDA2489

    Recall: Z-1116-2023 · Reported February 22, 2023

    Enforcement

    Recall Number
    Z-1116-2023
    Event ID
    91483
    Classification
    Class II
    Status
    Ongoing
    Product Type
    Devices
    Firm
    MEDLINE INDUSTRIES, LP - Northfield
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    February 22, 2023
    Initiation Date
    December 7, 2022
    Classification Date
    February 10, 2023
    Address
    3 Lakes Dr, N/A, Northfield, IL, 60093-2753, United States

    Description

    Surgical convenience kits labeled as: MEDLINE PLASTICS/PEDS KIT, Reorder Number DYNDA2489

    Reason

    The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile.

    Code Info

    GTIN 41093489695366, Lot # 22BMH128

    Distribution

    Nationwide

    Quantity

    480 units