RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026BaxterOfficial source

    Baxter Dialysis Machines recall in Canada: Leakage risk

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    In plain language

    This recall involves Baxter Artis, Phoenix, and Artis Physio dialysis machines sold in Canada. They are being recalled because using unvalidated connectors between the blood set and the patient's blood access may increase the risk of leakage or prevent a secure connection. Stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Check model numbers: Artis (112949), Phoenix (6022966700, 6023006700), Artis Physio (115965).
    • Contact Baxter for further instructions.

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    Affected products

    • Artis

      Model: 112949

      Lot: All lots

    • Phoenix

      Model: 6022966700, 6023006700

      Lot: All lots

    • Artis Physio

      Model: 115965

      Lot: All lots

    Why this matters

    Leakage 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: All lots

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 112949, 115965, 6022966700, 6023006700

    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.

    Want alerts if similar products are recalled in Canada?

    Frequently Asked Questions

    Why was this product recalled?

    Leakage risk

    What should consumers do?

    Stop using the product immediately. Check model numbers: Artis (112949), Phoenix (6022966700, 6023006700), Artis Physio (115965). Contact Baxter for further instructions.

    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. Leakage risk

    When was this product recalled?

    This product was recalled on December 11, 2020.

    Is the Baxter brand affected by this recall?

    Yes, Baxter products are affected by this recall. This recall involves Baxter Artis, Phoenix, and Artis Physio dialysis machines sold in Canada. They are being recalled because using unvalidated connectors between the blood set and the patient's blood access may increase the risk of leakage or prevent a secure connection. Stop using the product and follow the return/repair steps in the official notice.