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    Medical devicesUpdated Jan 3, 2026AzurionOfficial source

    Azurion 7M12, M20, B12 & B20 recall in Canada: electrical hazard

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    In plain language

    This recall involves Azurion 7M12, M20, B12 & B20 medical devices sold in Canada. They are being recalled because the power cable connection may not meet specifications, posing an electrical hazard. 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 if provided.
    • Return, repair, or dispose of it as instructed.

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    Affected products

    • Azurion 7 M12

      Model: 722 078

    • Azurion 7 M20

      Model: 722 079

    • Azurion 7 B12

      Model: 722 067

    • Azurion 7 B20

      Model: 722 068

    Why this matters

    Electrical hazard

    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 model number

      Model numbers are typically on the product label or packaging.

      Affected models: 722 067, 722 068, 722 078, 722 079

    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?

    Electrical hazard

    What should consumers do?

    Stop using the product immediately. Check model numbers if provided. Return, repair, or dispose of it as instructed.

    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. Electrical hazard

    When was this product recalled?

    This product was recalled on November 15, 2019.

    Is the Azurion brand affected by this recall?

    Yes, Azurion products are affected by this recall. This recall involves Azurion 7M12, M20, B12 & B20 medical devices sold in Canada. They are being recalled because the power cable connection may not meet specifications, posing an electrical hazard. Stop using the product and follow the return/repair steps in the official notice.