RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026DiaClonOfficial source

    DiaClon Rh-Subgroups + K (2019-06-17)

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    In plain language

    This recall involves DiaClon Rh-Subgroups + K medical devices sold in Canada. It's being recalled because a pink tint can affect automatic reading of blood test results. Stop using the product and follow the return steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Contact the manufacturer for more information.

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    Affected products

    • DiaClon Rh-Subgroups + K

      Model: 2124

      Lot: More than 10 numbers, contact manufacturer.

    Why this matters

    Incorrect test results

    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: 2124

    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 test results

    What should consumers do?

    Stop using the product immediately. Contact the manufacturer for more 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 test results

    When was this product recalled?

    This product was recalled on June 28, 2019.

    Is the DiaClon brand affected by this recall?

    Yes, DiaClon products are affected by this recall. This recall involves DiaClon Rh-Subgroups + K medical devices sold in Canada. It's being recalled because a pink tint can affect automatic reading of blood test results. Stop using the product and follow the return steps in the official notice.