RecallGuide.ca
    Medical devicesUpdated Feb 20, 2026Philips Medizin Systeme Boblingen GmbhOfficial source

    Philips IntelliVue Patient Monitors

    Share:

    In plain language

    This recall involves Philips IntelliVue Patient Monitors sold in Canada. They are being recalled because the alarm function may be unintentionally switched off, which could lead to delayed patient treatment. Healthcare professionals should contact the manufacturer for more information.

    What to do

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

    Get alerts for recalls like this

    Get email alerts when new recalls affect products in this category.

    Categories (optional)

    No spam. Unsubscribe anytime. We only email when there's a relevant recall.

    Affected products

    • IntelliVue MP40 Patient Monitor System - Main Unit

      Model: M8003A

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MX400 Patient Monitor

      Model: 866060

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MX850 Patient Monitor

      Model: 866470

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MP70 Patient Monitor System - Main Unit

      Model: M8007A

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MX Patient Monitor System - Main Unit

      Model: MX700, MX800

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MP60 Patient Monitor System - Main Unit

      Model: M8005A

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MP20 Patient Monitor System

      Model: M8001A

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MP5 Patient Monitor System - Main Unit

      Model: M8105A

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue X2 Multi-Measurement Module - Main Unit

      Model: M3002A

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MP90 Patient Monitor System - Main Unit

      Model: M8010A

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MP30 Patient Monitor System

      Model: M8002A

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MP80 Patient Monitor System - Main Unit

      Model: M8008A

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MP50 Patient Monitor System - Main Unit

      Model: M8004A

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MP2 Patient Monitor - Main Unit

      Model: M8102A

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MX550 Patient Monitor

      Model: 866066

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MX750 Patient Monitor

      Model: 866471

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MX500 Patient Monitor

      Model: 866064

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue Patient Monitor

      Model: 866062

      Lot: More than 10 numbers, contact manufacturer.

    • IntelliVue MX100 Patient Monitor

      Model: 867033

      Lot: More than 10 numbers, contact manufacturer.

    • X3 Multi-Measurement Module

      Model: 867030

      Lot: More than 10 numbers, contact manufacturer.

    Why this matters

    Delayed patient treatment due to monitor not alarming

    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: More than 10 numbers, contact manufacturer.

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 866060, 866062, 866064, 866066, 866470, 866471, 867030, 867033, M3002A, M8001A, M8002A, M8003A, M8004A, M8005A, M8007A, M8008A, M8010A, M8102A, M8105A, MX700, MX800

    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?

    Delayed patient treatment due to monitor not alarming

    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. Delayed patient treatment due to monitor not alarming

    When was this product recalled?

    This product was recalled on February 20, 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 Philips IntelliVue Patient Monitors sold in Canada. They are being recalled because the alarm function may be unintentionally switched off, which could lead to delayed patient treatment. Healthcare professionals should contact the manufacturer for more information.