Medical devicesUpdated Jan 3, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Official source

    Philips Azurion System recall in Canada: performance issues

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    In plain language

    This recall involves Philips Azurion 5 and Azurion 7 Systems used in healthcare settings in Canada. They are being recalled because they may lose imaging functionality and data, or continuously restart. Healthcare professionals should contact the manufacturer for more information.

    What to do

    • Contact the manufacturer if you require additional information.

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    Affected products

    • Azurion 7 M20

      Model: 722 079, 722 224

    • Azurion 7 B20

      Model: 722 068, 722 226

    • Azurion 5 M20

      Model: 722228

    • Azurion 7 B12

      Model: 722 067

    • Azurion 7 M12

      Model: 722 078, 722 223

    • Azurion 5 M12

      Model: 722 227

    Why this matters

    Loss of imaging functionality and data

    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, 722 223, 722 224, 722 226, 722 227, 722228

    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?

    Loss of imaging functionality and data

    What should consumers do?

    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?

    Yes, there may be a health risk. Loss of imaging functionality and data

    When was this product recalled?

    This product was recalled on January 5, 2024.

    Is the PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. brand affected by this recall?

    Yes, PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. products are affected by this recall. This recall involves Philips Azurion 5 and Azurion 7 Systems used in healthcare settings in Canada. They are being recalled because they may lose imaging functionality and data, or continuously restart. Healthcare professionals should contact the manufacturer for more information.