Medical devicesUpdated Jan 3, 2026B. Braun Avitum AgOfficial source

    DiaStream Classic HD SNCO recall in Canada: Sterility issue

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    In plain language

    This recall involves the DiaStream Classic HD SNCO, a medical device sold in Canada. It's being recalled because of a sterility issue, as a particle may be present in the venous expansion chamber. Stop using the product and contact the importer/supplier for further instructions.

    What to do

    • Stop using the product immediately.
    • Contact the importer/supplier.

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    Affected products

    • DiaStream Classic HD SNCO

      Model: 7211349

      Lot: 22E17534P

    Why this matters

    Sterility issue

    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: 22E17534P

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 7211349

    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?

    Sterility issue

    What should consumers do?

    Stop using the product immediately. Contact the importer/supplier.

    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. Sterility issue

    When was this product recalled?

    This product was recalled on March 25, 2025.

    Is the B. Braun Avitum Ag brand affected by this recall?

    Yes, B. Braun Avitum Ag products are affected by this recall. This recall involves the DiaStream Classic HD SNCO, a medical device sold in Canada. It's being recalled because of a sterility issue, as a particle may be present in the venous expansion chamber. Stop using the product and contact the importer/supplier for further instructions.