RecallGuide.ca
    Health products••Updated Mar 17, 2026•PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.•Official source

    Allura Xper and Azurion Systems

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    In plain language

    This recall involves Philips Allura Xper and Azurion Systems sold in Canada. They are being recalled because the X-ray imaging may not start or may work intermittently. This issue could cause delays or stop medical procedures. Stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Contact the manufacturer for additional information.

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    Affected products

    • Allura Xper FD10 (Product Of AlluraClarity Family)

      Model: 722026

    • Allura Xper FD10/10 (Product Of AlluraClarity Family)

      Model: 722027

    • Azurion 7 M20

      Model: 722 079, 722 224, 722234

    • Allura Xper FD20/15

      Model: 722058

    • Allura Xper FD10

      Model: 001443

    • Allura Xper FD20/10 (Product Of AlluraClarity Family)

      Model: 722029

    • Azurion 7 M12

      Model: 722 078, 722 223, 722233

    • Azurion 3 M12

      Model: 722 063, 722 221, 722229

    • Azurion 5 M12

      Model: 722 227, 722231

    • Azurion 5 M20

      Model: 722 228, 722232

    • Allura Xper FD20 (Product Of AlluraClarity Family)

      Model: 722028

    • Allura Xper FD20/20 (Product Of AlluraClarity Family)

      Model: 722038

    • Azurion 7 B20

      Model: 722 068, 722 226, 722236

    • Azurion 3 M15

      Model: 722 064, 722 222, 722230

    • Azurion 7 B12

      Model: 722 067, 722 225, 722235

    • Allura Xper FD20 Or Table (Product Of AlluraClarity Family)

      Model: 722035

    Why this matters

    Delay or abort of procedure

    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: 001443, 722 063, 722 064, 722 067, 722 068, 722 078, 722 079, 722 221, 722 222, 722 223, 722 224, 722 225, 722 226, 722 227, 722 228, 722026, 722027, 722028, 722029, 722035, 722038, 722058, 722229, 722230, 722231, 722232, 722233, 722234, 722235, 722236

    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.

    Want alerts if similar products are recalled in Canada?

    Frequently Asked Questions

    Why was this product recalled?

    Delay or abort of procedure

    What should consumers do?

    Stop using the product immediately. Contact the manufacturer for 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. Delay or abort of procedure

    When was this product recalled?

    This product was recalled on March 17, 2026.

    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 Allura Xper and Azurion Systems sold in Canada. They are being recalled because the X-ray imaging may not start or may work intermittently. This issue could cause delays or stop medical procedures. Stop using the product and follow the return/repair steps in the official notice.