BEUDAMED
    FDA Recall Open, Classified

    Medline Kits containing Codman Disposable Perforator 14 mm: CRANIOTOMY, SKU DYNJ35349C

    Recall: Z-1810-2025 · Initiated April 22, 2025

    Recall

    Recall Number
    Z-1810-2025
    Event Number
    96821
    Firm
    MEDLINE INDUSTRIES, LP Northfield
    FEI Number
    1417592
    Product Code
    OJG
    Status
    Open, Classified
    Root Cause
    Nonconforming Material/Component
    Initiated
    April 22, 2025
    Posted
    May 31, 2025
    Address
    3 Lakes Dr, Northfield, IL, 60093-2753

    Description

    Medline Kits containing Codman Disposable Perforator 14 mm: CRANIOTOMY, SKU DYNJ35349C

    Reason

    Affected kits contain recalled Integra Lifesciences Codman Disposable Perforators due to inadequate welds on specific lots. Perforators with inadequate welds may break or separate.

    Action

    On April 22, 2025, the firm notified customers of the recall through letters titled Immediate Action Required Voluntary Medical Device Recall. Customers were instructed to identify and quarantine all affected product on hand. Customers are to submit a response form to the recalling firm. Upon receipt of the response firm, Medline will provide the customer with over-labels to place on affected inventory, which will include instructions for staff to remove and discard the affected component prior to using the kit. Distributors should notify downstream customers/accounts of this recall. If you have any questions, contact the Recall Department at 866-359-1704 or [email protected].

    Distribution

    US distribution to CA, FL, IL, IN, KY, MA, MD, MN, NY, TX, VT, WA and WI. No OUS distribution.

    Quantity

    1853 total