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    Medical devicesUpdated Jan 3, 2026Alaris SystemOfficial source

    Alaris System recall in Canada: potential hardware issues

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    In plain language

    This recall involves various Alaris System modules sold in Canada. It's being recalled because of four hardware situations that require user attention and actions, including damaged connectors and improperly secured batteries. 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 if provided.
    • Contact the manufacturer for more information.
    • Follow the return or repair instructions provided by the manufacturer.

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    Affected products

    • Alaris System - ID Module

      Model: 8.4.5.0

      Lot: More than 10 numbers, contact manufacturer.

    • Alaris System - Server Mobile Systems Manager

      Model: 8000 8015

      Lot: More than 10 numbers, contact manufacturer.

    • Alaris System - PCA Module

      Model: 8120

      Lot: More than 10 numbers, contact manufacturer.

    • Alaris System - Entidal CO2 Module

      Model: 8300

      Lot: More than 10 numbers, contact manufacturer.

    • Alaris System - Pump

      Model: 8100

      Lot: More than 10 numbers, contact manufacturer.

    • Alaris System - SpO2 Module

      Model: 8210 8220

      Lot: More than 10 numbers, contact manufacturer.

    • Alaris System - Syringe Pump Module

      Model: 8110

      Lot: More than 10 numbers, contact manufacturer.

    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: 8.4.5.0, 8000 8015, 8100, 8110, 8120, 8210 8220, 8300

    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?

    This recall involves various Alaris System modules sold in Canada. It's being recalled because of four hardware situations that require user attention and actions, including damaged connectors and improperly secured batteries. Stop using the product and follow the return/repair steps in the official notice.

    What should consumers do?

    Stop using the product immediately. Check model numbers if provided. Contact the manufacturer for more information. Follow the return or repair instructions provided by the manufacturer.

    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?

    A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.

    When was this product recalled?

    This product was recalled on July 17, 2020.

    Is the Alaris System brand affected by this recall?

    Yes, Alaris System products are affected by this recall. This recall involves various Alaris System modules sold in Canada. It's being recalled because of four hardware situations that require user attention and actions, including damaged connectors and improperly secured batteries. Stop using the product and follow the return/repair steps in the official notice.