RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026AXIUSOfficial source

    Blower/Mister recall in Canada: May cause procedural delay

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    In plain language

    This recall involves the AXIUS Blower Mister medical device sold in Canada. It's being recalled because it may fail to emit carbon dioxide (CO2), which could lead to procedural delays during off-pump coronary artery bypass (OPCAB) surgery. Stop using the product and follow the return/repair steps in the official notice.

    What to do

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

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    Affected products

    • Blower/Mister

      Model: CB-1000

      Lot: 96255607

    Why this matters

    Procedural delay

    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: 96255607

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: CB-1000

    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?

    Procedural delay

    What should consumers do?

    Stop using the product immediately. Check model/serial 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. Procedural delay

    When was this product recalled?

    This product was recalled on February 15, 2019.

    Is the AXIUS brand affected by this recall?

    Yes, AXIUS products are affected by this recall. This recall involves the AXIUS Blower Mister medical device sold in Canada. It's being recalled because it may fail to emit carbon dioxide (CO2), which could lead to procedural delays during off-pump coronary artery bypass (OPCAB) surgery. Stop using the product and follow the return/repair steps in the official notice.