BEUDAMED
    FDA Recall Terminated

    KWIK-STIK" plus: Clostridium perfringens

    Recall: Z-1125-2022 · Initiated May 6, 2022

    Recall

    Recall Number
    Z-1125-2022
    Event Number
    90150
    Firm
    Microbiologics Inc
    FEI Number
    2150138
    Product Code
    JTR
    Status
    Terminated
    Root Cause
    Labeling mix-ups
    Initiated
    May 6, 2022
    Terminated
    January 16, 2024
    Address
    200 Cooper Ave N, Saint Cloud, MN, 56303-4440

    Description

    KWIK-STIK" plus: Clostridium perfringens

    Reason

    Labeling error.

    Action

    The firm issued a recall notification to the consignees beginning on 05/06/2022 via email. The letter informs the consignee to inspect inventory, review lab procedures, use or discard affected product depending on lab procedures, and complete the response form.

    Distribution

    Distributed US Nationwide to IA, TN and internationally to Mexico, Colombia, France, South Africa, United Kingdom.

    Quantity

    8 units