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

    Allura Xper Fd10 & Fd20 recall in Canada: Mechanical defect

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    In plain language

    This recall involves Allura Xper Fd10 and Fd20 products sold in Canada. They are being recalled because a mechanical defect in the cooling system could cause damage to the system. 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 Fd10/10 (Product Of Alluraclarity Family)

      Model: 722027

      Lot: Not applicable

    • Allura Xper Fd10 (Product Of Alluraclarity Family)

      Model: 722026

      Lot: Not applicable

    • Allura Xper Fd10

      Model: 001443

      Lot: Not applicable

    • Allura Xper Fd20 (Product Of Alluraclarity Family)

      Model: 722028

      Lot: Not applicable

    Why this matters

    Mechanical defect

    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: Not applicable

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 001443, 722026, 722027, 722028

    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?

    Mechanical defect

    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. Mechanical defect

    When was this product recalled?

    This product was recalled on December 13, 2021.

    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 Allura Xper Fd10 and Fd20 products sold in Canada. They are being recalled because a mechanical defect in the cooling system could cause damage to the system. Contact the manufacturer for more information.