RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026Smiths MedicalOfficial source

    CADD-Solis™ Ambulatory Infusion Pump recall in Canada: performance issues

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    In plain language

    This recall involves CADD-Solis™ Ambulatory Infusion Pumps sold in Canada. They are being recalled due to performance issues that could cause melting of plastic housing or electrical shorts. Stop using the product and contact the manufacturer for more information.

    What to do

    • Stop using the product immediately.
    • Contact Smiths Medical ASD, Inc. for additional information.

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    Affected products

    • CADD-Solis™ Ambulatory Infusion Pump

      Model: 21-2101-0200-02, 21-2101-51, 21-2102-51, 21-2111-0100-51, 21-2111-0200-02, 21-2111-0300-00, 21-2111-0300-02, 21-2111-0300-50, 21-2111-0400-51, 21-2111-0401-51, 21-2111-0403-02, 21-2111-0403-51, 21-2111-0403-78, 21-2112-0100-51, 21-2112-0200-02, 21-2112-0300-02, 21-2112-0300-50, 21-2112-0400-51, 21-2112-0401-51, 21-2112-0403-02, 21-2112-0403-51, 21-2112-0403-78

      Lot: More than 10 numbers, contact manufacturer.

    • CADD-Solis VIP™ Ambulatory Infusion Pump

      Model: 21-2120-0100-02, 21-2120-0100-50, 21-2120-0100-51, 21-2120-0100-95, 21-2120-0102 -02, 21-2120-0102-51, 21-2120-0102-78, 21-2120-0102-92, 21-2120-0103-02, 21-2120-0103-51, 21-2120-0103-78

      Lot: More than 10 numbers, contact manufacturer.

    Why this matters

    Electrical short, melting plastic

    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: 21-2101-0200-02, 21-2101-51, 21-2102-51, 21-2111-0100-51, 21-2111-0200-02, 21-2111-0300-00, 21-2111-0300-02, 21-2111-0300-50, 21-2111-0400-51, 21-2111-0401-51, 21-2111-0403-02, 21-2111-0403-51, 21-2111-0403-78, 21-2112-0100-51, 21-2112-0200-02, 21-2112-0300-02, 21-2112-0300-50, 21-2112-0400-51, 21-2112-0401-51, 21-2112-0403-02, 21-2112-0403-51, 21-2112-0403-78, 21-2120-0100-02, 21-2120-0100-50, 21-2120-0100-51, 21-2120-0100-95, 21-2120-0102 -02, 21-2120-0102-51, 21-2120-0102-78, 21-2120-0102-92, 21-2120-0103-02, 21-2120-0103-51, 21-2120-0103-78

    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?

    Electrical short, melting plastic

    What should consumers do?

    Stop using the product immediately. Contact Smiths Medical ASD, Inc. 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. Electrical short, melting plastic

    When was this product recalled?

    This product was recalled on April 28, 2025.

    Is the Smiths Medical brand affected by this recall?

    Yes, Smiths Medical products are affected by this recall. This recall involves CADD-Solis™ Ambulatory Infusion Pumps sold in Canada. They are being recalled due to performance issues that could cause melting of plastic housing or electrical shorts. Stop using the product and contact the manufacturer for more information.