RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026IntelliVue, IntelliBridgeOfficial source

    IntelliVue and IntelliBridge recall in Canada: incorrect data display

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    In plain language

    This recall involves IntelliVue Information Centre iX Software and IntelliBridge Systems sold in Canada. They are being recalled because they may display patient data at 100 times the actual value under specific regional settings. Stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Check model numbers M3290B (IntelliVue) and 866417 (IntelliBridge).
    • Contact Philips Medical Systems for instructions.

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    Affected products

    • IntelliVue -Information Centre iX - Software

      Model: M3290B

      Lot: All lots

    • IntelliBridge System

      Model: 866417

      Lot: All lots

    Why this matters

    Incorrect data display leading to potential medical errors

    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: All lots

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 866417, M3290B

    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?

    Incorrect data display leading to potential medical errors

    What should consumers do?

    Stop using the product immediately. Check model numbers M3290B (IntelliVue) and 866417 (IntelliBridge). Contact Philips Medical Systems for instructions.

    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. Incorrect data display leading to potential medical errors

    When was this product recalled?

    This product was recalled on May 17, 2019.

    Is the IntelliVue, IntelliBridge brand affected by this recall?

    Yes, IntelliVue, IntelliBridge products are affected by this recall. This recall involves IntelliVue Information Centre iX Software and IntelliBridge Systems sold in Canada. They are being recalled because they may display patient data at 100 times the actual value under specific regional settings. Stop using the product and follow the return/repair steps in the official notice.