BEUDAMED
    FDA Recall Open, Classified

    Medline convenience kits labeled as: a. MIDDLE EAR PACK-LF, Model DYNJ0689093V, b. EENT PACK, Model Number DYNJ62927 Model/Catalog Number: a. DYNJ0689093V, b. DYNJ62927

    Recall: Z-1472-2022 · Initiated June 6, 2022

    Recall

    Recall Number
    Z-1472-2022
    Event Number
    90516
    Firm
    MEDLINE INDUSTRIES, LP SPT
    FEI Number
    3000717925
    Product Code
    OGR
    Status
    Open, Classified
    Root Cause
    Under Investigation by firm
    Initiated
    June 6, 2022
    Address
    1170 S Northpoint Blvd, Waukegan, IL, 60085-6757

    Description

    Medline convenience kits labeled as: a. MIDDLE EAR PACK-LF, Model DYNJ0689093V, b. EENT PACK, Model Number DYNJ62927 Model/Catalog Number: a. DYNJ0689093V, b. DYNJ62927

    Reason

    Kits contain leaking bottles of isopropyl alcohol

    Action

    The firm's consignees were notified by US mail on 06/06/2022 and instructed to destroy any affected kits on hand in accordance with their local and state regulations.

    Distribution

    US Nationwide distribution.

    Quantity

    477 units