BEUDAMED
    FDA Recall Open, Classified

    Medline medical procedure kits labeled as follows: a) BASIC NEURO, REF DYNJ909171A; b) NEURO, REF DYNJ905510D; c) NEURO, REF DYNJ902388L; d) NEURO SAS, REF DYNJ908566

    Recall: Z-2711-2024 · Initiated March 22, 2024

    Recall

    Recall Number
    Z-2711-2024
    Event Number
    94356
    Firm
    MEDLINE INDUSTRIES, LP Northfield
    FEI Number
    1417592
    Product Code
    OJG
    Status
    Open, Classified
    Root Cause
    Under Investigation by firm
    Initiated
    March 22, 2024
    Posted
    August 22, 2024
    Address
    3 Lakes Dr, Northfield, IL, 60093-2753

    Description

    Medline medical procedure kits labeled as follows: a) BASIC NEURO, REF DYNJ909171A; b) NEURO, REF DYNJ905510D; c) NEURO, REF DYNJ902388L; d) NEURO SAS, REF DYNJ908566

    Reason

    A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.

    Action

    Medline Industries issued a Safety Alert to its consignees on 03/22/2024 via email and certified mail. The notice explained the problem with the device and requested that consignees follow the instructions for use. Distributors or those who further transferred the affected product were directed to notify their consignees.

    Distribution

    Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.

    Quantity

    2013 units