RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026BECKMAN COULTER, INC.Official source

    UniCel DxI 600 & 800 Systems recall in Canada: Performance issue

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    In plain language

    This recall involves UniCel DxI 600 & 800 Systems sold in Canada. It's being recalled because of a software issue that can cause increased motion errors. This recall is for healthcare professionals.

    What to do

    • Contact the manufacturer for more information.

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    Affected products

    • UniCel DxI 600 Access Immunoassay Analyzer

      Model: A30260

      Lot: 902385, 902386, 902475, 902622, 902624

    • DxI 600 Access Immunoassay W/Spot B

      Model: A71460

      Lot: More than 10 numbers, contact manufacturer.

    • UniCel DxI 800 Access Immunoassay Analyzer

      Model: 973100

      Lot: 609576

    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: 609576, 902385, 902386, 902475, 902622, 902624, More than 10 numbers, contact manufacturer.

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 973100, A30260, A71460

    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?

    This recall involves UniCel DxI 600 & 800 Systems sold in Canada. It's being recalled because of a software issue that can cause increased motion errors. This recall is for healthcare professionals.

    What should consumers do?

    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?

    A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.

    When was this product recalled?

    This product was recalled on July 16, 2025.

    Is the BECKMAN COULTER, INC. brand affected by this recall?

    Yes, BECKMAN COULTER, INC. products are affected by this recall. This recall involves UniCel DxI 600 & 800 Systems sold in Canada. It's being recalled because of a software issue that can cause increased motion errors. This recall is for healthcare professionals.