Medical devicesUpdated Jan 3, 2026Philips Medizin Systeme Boeblingen GmbHOfficial source

    Patient Information Center iX recall in Canada: Medical device performance issue

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    In plain language

    This recall involves the Patient Information Center iX, versions 4.0 and 4.1, sold in Canada. It's being recalled because a mobile application issue could delay patient treatment. Healthcare providers should contact the manufacturer for more information.

    What to do

    • Contact the manufacturer if you require additional information.

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    Affected products

    • Patient Information Center iX

      Model: VERSION 4.0, VERSION 4.1

    Why this matters

    Delay in treatment for patients

    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: VERSION 4.0, VERSION 4.1

    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?

    Delay in treatment for patients

    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. Delay in treatment for patients

    When was this product recalled?

    This product was recalled on March 14, 2024.

    Is the Philips Medizin Systeme Boeblingen GmbH brand affected by this recall?

    Yes, Philips Medizin Systeme Boeblingen GmbH products are affected by this recall. This recall involves the Patient Information Center iX, versions 4.0 and 4.1, sold in Canada. It's being recalled because a mobile application issue could delay patient treatment. Healthcare providers should contact the manufacturer for more information.