RecallGuide.ca
    Health productsUpdated Mar 11, 2026Philips Medizin Systeme Boblingen GmbhOfficial source

    IntelliVue MX Patient Monitor System-IntelliBridge Module EC10

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    In plain language

    This recall involves the IntelliVue MX Patient Monitor System-IntelliBridge Module EC10 sold in Canada. It's being recalled because it may fail to alarm for "No Device Data" when connected to a Hamilton ventilator. Healthcare professionals should contact the manufacturer for more information.

    What to do

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

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    Affected products

    • IntelliVue MX Patient Monitor System-IntelliBridge Module EC10

      Model: 865115

      Lot: Not applicable

    Why this matters

    Monitoring risk due to alarm failure

    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: 865115

    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?

    Monitoring risk due to alarm failure

    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. Monitoring risk due to alarm failure

    When was this product recalled?

    This product was recalled on March 11, 2026.

    Is the Philips Medizin Systeme Boblingen Gmbh brand affected by this recall?

    Yes, Philips Medizin Systeme Boblingen Gmbh products are affected by this recall. This recall involves the IntelliVue MX Patient Monitor System-IntelliBridge Module EC10 sold in Canada. It's being recalled because it may fail to alarm for "No Device Data" when connected to a Hamilton ventilator. Healthcare professionals should contact the manufacturer for more information.