RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026ADVIA CentaurOfficial source

    ADVIA Centaur CP System recall in Canada: inaccurate test results

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    In plain language

    This recall involves various ADVIA Centaur CP System and ADVIA Centaur System assays used in medical testing in Canada. They are being recalled because biotin interference can lead to inaccurate test results. Healthcare professionals should stop using the affected products and follow the instructions from Siemens Healthcare Diagnostics.

    What to do

    • Stop using the affected assays immediately.
    • Check the model or catalog numbers of your ADVIA Centaur assays.
    • Follow the instructions provided by Siemens Healthcare Diagnostics regarding this recall.

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    Affected products

    Specific affected products are listed in the official notice.

    Why this matters

    Inaccurate test results

    Do I have this product?

    This recall applies to specific products. Details are listed in the official notice.

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    Frequently Asked Questions

    Why was this product recalled?

    Inaccurate test results

    What should consumers do?

    Stop using the affected assays immediately. Check the model or catalog numbers of your ADVIA Centaur assays. Follow the instructions provided by Siemens Healthcare Diagnostics regarding this recall.

    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. Inaccurate test results

    When was this product recalled?

    This product was recalled on January 29, 2018.

    Is the ADVIA Centaur brand affected by this recall?

    Yes, ADVIA Centaur products are affected by this recall. This recall involves various ADVIA Centaur CP System and ADVIA Centaur System assays used in medical testing in Canada. They are being recalled because biotin interference can lead to inaccurate test results. Healthcare professionals should stop using the affected products and follow the instructions from Siemens Healthcare Diagnostics.