RecallGuide.ca
    Health productsUpdated Jan 3, 2026BaxterOfficial source

    Baxter intravenous solutions recall in Canada: potential leak

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    In plain language

    This recall involves Baxter's 0.9% Sodium Chloride Injection, USP and Lactated Ringer’s Injection, USP sold in Canada. They are being recalled because certain lots may leak when administered under pressure infusion. Stop using affected products under pressure and follow the instructions in the official notice.

    What to do

    • Stop using affected lots of these products under pressure infusion.
    • Inspect bags for leaks before and during use.
    • Discard any bags that show signs of leakage.
    • Consult your healthcare professional if you have questions or concerns.

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    Affected products

    Specific affected products are listed in the official notice.

    Why this matters

    Risk of infection or inaccurate medication delivery

    Do I have this product?

    This recall applies to specific products. Details are listed in the official notice.

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    Frequently Asked Questions

    Why was this product recalled?

    Risk of infection or inaccurate medication delivery

    What should consumers do?

    Stop using affected lots of these products under pressure infusion. Inspect bags for leaks before and during use. Discard any bags that show signs of leakage. Consult your healthcare professional if you have questions or concerns.

    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. Risk of infection or inaccurate medication delivery

    When was this product recalled?

    This product was recalled on March 9, 2022.

    Is the Baxter brand affected by this recall?

    Yes, Baxter products are affected by this recall. This recall involves Baxter's 0.9% Sodium Chloride Injection, USP and Lactated Ringer’s Injection, USP sold in Canada. They are being recalled because certain lots may leak when administered under pressure infusion. Stop using affected products under pressure and follow the instructions in the official notice.