RecallGuide.ca
    Medical devices••Updated Jan 3, 2026•PHILIPS MEDICAL SYSTEMS NEDERLAND•Official source

    Allura Xper Systems recall in Canada: performance issues

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    In plain language

    This recall involves Philips Allura Xper Systems sold in Canada. They are being recalled because internal components may deteriorate, affecting system performance. 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

    • Allura Xper FD10

      Model: 001443

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

      Model: 722029

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

      Model: 722035

    • Allura Xper FD20 (Product Of AlluraClarity Family)

      Model: 722028

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

      Model: 722038

    • Allura Xper FD20/15 Or Table

      Model: 722 059

    • Allura Xper FD 10 (Product Of AlluraClarity Family)

      Model: 722026

    • Allura Xper FD10 Or Table (Product Of AlluraClarity Family)

      Model: 722033

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

      Model: 722027

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

      Model: 722039

    • Allura Xper FD20/15

      Model: 722058

    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, 722 059, 722026, 722027, 722028, 722029, 722033, 722035, 722038, 722039, 722058

    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?

    This recall involves Philips Allura Xper Systems sold in Canada. They are being recalled because internal components may deteriorate, affecting system performance. Healthcare professionals should contact the manufacturer for more information.

    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?

    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 September 24, 2025.

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

    Yes, PHILIPS MEDICAL SYSTEMS NEDERLAND products are affected by this recall. This recall involves Philips Allura Xper Systems sold in Canada. They are being recalled because internal components may deteriorate, affecting system performance. Healthcare professionals should contact the manufacturer for more information.