RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026Carefusion 303, Inc.Official source

    Alaris™ Pump Module recall in Canada: Device compatibility issue

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    In plain language

    This recall involves Alaris™ Pump Module and BD Alaris™ Pump Module in Canada. It's being recalled because of a device compatibility issue that could lead to incorrect infusion. This recall is for healthcare professionals. Contact the manufacturer for more information.

    What to do

    • Contact the manufacturer if you require additional information.

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    Affected products

    • Alaris™ Pump Module & BD Alaris™ Pump Module

      Model: 8100

      Lot: More than 10 numbers, contact manufacturer.

    Why this matters

    Incorrect infusion

    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: 8100

    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?

    Incorrect infusion

    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. Incorrect infusion

    When was this product recalled?

    This product was recalled on July 22, 2025.

    Is the Carefusion 303, Inc. brand affected by this recall?

    Yes, Carefusion 303, Inc. products are affected by this recall. This recall involves Alaris™ Pump Module and BD Alaris™ Pump Module in Canada. It's being recalled because of a device compatibility issue that could lead to incorrect infusion. This recall is for healthcare professionals. Contact the manufacturer for more information.