Medical devicesUpdated Jan 3, 2026Microtek Medical IncOfficial source

    Microtek Decanter Devices recall in Canada: Sterility and unauthorized device

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    In plain language

    This recall involves Microtek Decanter Devices sold in Canada. They are being recalled because some packaging has pinholes and tears, which could affect sterility. Also, these devices are not licensed for use in Canada. Stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Check the model and lot numbers if you have these devices.
    • Contact the manufacturer for more information.

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    Affected products

    • Transfer Device

      Model: 2008S

      Lot: 170828, 231027

    • Vial Decanter

      Model: 2006S

      Lot: 231230, 180620

    • Bottle Decanter

      Model: 2004S

      Lot: 180625, 221220

    • C-Flo Bag Decanter

      Model: 2000S

      Lot: 180122, 240110

    • Bag Decanter II

      Model: 2002S

      Lot: 240219, 170216

    Why this matters

    Sterility risk

    Do I have this product?

    This recall only applies to specific products. Follow the steps below to check.

    1. 1

      Check the product name

      Make sure your product name matches one of the affected products listed above.

    2. 2

      Check the lot number

      Lot numbers identify specific production batches.

      Affected lots: 170828, 231027, 180122, 240110, 180625, 221220, 231230, 180620, 240219, 170216

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 2000S, 2002S, 2004S, 2006S, 2008S

    If your product matches one or more of the details above, it may be affected by this recall.

    If your product does not match these details, it is not affected by this recall.

    When in doubt, always check the official notice.

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    Frequently Asked Questions

    Why was this product recalled?

    Sterility risk

    What should consumers do?

    Stop using the product immediately. Check the model and lot numbers if you have these devices. Contact the manufacturer for more information.

    Where was the product sold?

    This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.

    Is there a health risk?

    Yes, there may be a health risk. Sterility risk

    When was this product recalled?

    This product was recalled on June 14, 2024.

    Is the Microtek Medical Inc brand affected by this recall?

    Yes, Microtek Medical Inc products are affected by this recall. This recall involves Microtek Decanter Devices sold in Canada. They are being recalled because some packaging has pinholes and tears, which could affect sterility. Also, these devices are not licensed for use in Canada. Stop using the product and follow the return/repair steps in the official notice.