Medical devicesUpdated Jan 3, 2026Smiths Medical Asd Inc.Official source

    ParaPAC Plus 310 recall in Canada: performance issue

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    In plain language

    This recall involves the ParaPAC Plus 310, a medical device used for ventilation. It's being recalled because the patient outlet connector may loosen or detach, affecting its function. Healthcare professionals should contact the manufacturer for more information.

    What to do

    • Contact the manufacturer if you require additional information.

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    Affected products

    • ParaPAC Plus 310

      Model: P310NCA, P310NCAFREN, P310NUS

      Lot: Not applicable.

    Why this matters

    Performance issue affecting active ventilation function

    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: P310NCA, P310NCAFREN, P310NUS

    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?

    Performance issue affecting active ventilation function

    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. Performance issue affecting active ventilation function

    When was this product recalled?

    This product was recalled on July 2, 2024.

    Is the Smiths Medical Asd Inc. brand affected by this recall?

    Yes, Smiths Medical Asd Inc. products are affected by this recall. This recall involves the ParaPAC Plus 310, a medical device used for ventilation. It's being recalled because the patient outlet connector may loosen or detach, affecting its function. Healthcare professionals should contact the manufacturer for more information.