BEUDAMED
    FDA Recall Open, Classified

    BLOOD CULTURE KIT, REF DYNDH1647B

    Recall: Z-0314-2024 · Initiated November 1, 2023

    Recall

    Recall Number
    Z-0314-2024
    Event Number
    93379
    Firm
    MEDLINE INDUSTRIES, LP Northfield
    FEI Number
    1417592
    Product Code
    OIB
    Status
    Open, Classified
    Root Cause
    Under Investigation by firm
    Initiated
    November 1, 2023
    Posted
    November 16, 2023
    Address
    3 Lakes Dr, Northfield, IL, 60093-2753

    Description

    BLOOD CULTURE KIT, REF DYNDH1647B

    Reason

    This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.

    Action

    Medline Industries issued a MEDICAL DEVICE RECALL notice to its consignees on 11/01/2023 via email. The notice explained the issue and requested that the destruction of the affected kits. Consignees were also instructed to notify all parties if the kits were transferred.

    Distribution

    US Nationwide distribution in the state of California.

    Quantity

    1890 kits