Medical devicesUpdated Jan 3, 2026Diasorin Inc.Official source

    Liaison Q.S.E.T. Device Plus recall in Canada: labelling and packaging issue

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    In plain language

    This recall involves the Liaison Q.S.E.T. Device Plus sold in Canada. It's being recalled because of a labelling and packaging issue that may cause buffer leakage. Stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Check the lot or serial numbers provided.
    • Follow the manufacturer's instructions for inspecting and disposing of affected devices.

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    Affected products

    • Liaison Q.S.E.T. Device Plus

      Lot: 229224, 225084, 217134, 224124, 221294, 230094, 210204, 223274, 224244, 232094, 234114, 221214, 236174, 259144, 228174, 319060

    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: 229224, 225084, 217134, 224124, 221294, 230094, 210204, 223274, 224244, 232094, 234114, 221214, 236174, 259144, 228174, 319060

    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?

    This recall involves the Liaison Q.S.E.T. Device Plus sold in Canada. It's being recalled because of a labelling and packaging issue that may cause buffer leakage. Stop using the product and follow the return/repair steps in the official notice.

    What should consumers do?

    Stop using the product immediately. Check the lot or serial numbers provided. Follow the manufacturer's instructions for inspecting and disposing of affected devices.

    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?

    A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.

    When was this product recalled?

    This product was recalled on December 4, 2024.

    Is the Diasorin Inc. brand affected by this recall?

    Yes, Diasorin Inc. products are affected by this recall. This recall involves the Liaison Q.S.E.T. Device Plus sold in Canada. It's being recalled because of a labelling and packaging issue that may cause buffer leakage. Stop using the product and follow the return/repair steps in the official notice.