RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026Official source

    Drop Admin Set recall in Canada: incorrect drip rate

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    In plain language

    This recall involves the Drop Admin Set sold in Canada. It's being recalled because some sets may have an incorrect drip cannula, leading to an inaccurate drip rate. Stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Check model and lot numbers.
    • Contact ICU Medical for further instructions.

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    Affected products

    • Drop Admin Set

      Model: B30211

      Lot: 4168832

    Why this matters

    Incorrect medication delivery

    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: 4168832

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: B30211

    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?

    Incorrect medication delivery

    What should consumers do?

    Stop using the product immediately. Check model and lot numbers. Contact ICU Medical for further instructions.

    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 medication delivery

    When was this product recalled?

    This product was recalled on October 18, 2019.