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    Medical devicesUpdated Jan 3, 2026Synovis Life Technologies, Inc.Official source

    Synovis medical devices recall in Canada: labelling issue

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    In plain language

    This recall involves Synovis Intravascular Probes, Shunts, and Patches sold in Canada. They are being recalled because marketing brochures contain inaccurate content that does not align with the products' instructions for use. This recall is for healthcare professionals.

    What to do

    • Discard all copies of the marketing brochure (Ref ca-as32-210022 (English) and ca-as32-220004 (French)).
    • Contact the manufacturer if you require additional information.

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    Affected products

    Specific affected products are listed in the official notice.

    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?

    This recall involves Synovis Intravascular Probes, Shunts, and Patches sold in Canada. They are being recalled because marketing brochures contain inaccurate content that does not align with the products' instructions for use. This recall is for healthcare professionals.

    What should consumers do?

    Discard all copies of the marketing brochure (Ref ca-as32-210022 (English) and ca-as32-220004 (French)). Contact the manufacturer if you require additional 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?

    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 1, 2023.

    Is the Synovis Life Technologies, Inc. brand affected by this recall?

    Yes, Synovis Life Technologies, Inc. products are affected by this recall. This recall involves Synovis Intravascular Probes, Shunts, and Patches sold in Canada. They are being recalled because marketing brochures contain inaccurate content that does not align with the products' instructions for use. This recall is for healthcare professionals.