RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026ArtisOfficial source

    Artis Zeego System recall in Canada: software issues

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    In plain language

    This recall involves Artis Zeego and Artis Zee medical systems sold in Canada. They are being recalled because software issues could block system movements. Healthcare professionals should stop using the affected products and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Check model and serial numbers.
    • Contact Siemens Healthcare GMBH for repair or reactivation.

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    Affected products

    • ARTIS ZEEGO MULTI-AXIS

      Model: 10280959

      Lot: 160846, 161205

    • ARTIS ZEE FLOOR

      Model: 10094135

      Lot: 124222, 136972, 137423

    • ARTIS ZEE CEILING

      Model: 10094137

      Lot: 147638, 147832, 147908, 148012, 148024, 148204, 148244, 148304

    • ARTIS ZEE BIPLANE

      Model: 10094141

      Lot: 153810, 154679

    • ARTIS Q

      Model: 10848280, 10848281, 10848282, 10848283

      Lot: More than 10 numbers, contact manufacturer.

    • ARTIS Q.ZEN MODULAR ANGIOGRAPHIC SYSTEM

      Model: 10848355

      Lot: 123048, 123214

    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: 123048, 123214, 124222, 136972, 137423, 147638, 147832, 147908, 148012, 148024, 148204, 148244, 148304, 153810, 154679, 160846, 161205, More than 10 numbers, contact manufacturer.

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 10094135, 10094137, 10094141, 10280959, 10848280, 10848281, 10848282, 10848283, 10848355

    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 Artis Zeego and Artis Zee medical systems sold in Canada. They are being recalled because software issues could block system movements. Healthcare professionals should stop using the affected products and follow the return/repair steps in the official notice.

    What should consumers do?

    Stop using the product immediately. Check model and serial numbers. Contact Siemens Healthcare GMBH for repair or reactivation.

    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 October 9, 2020.

    Is the Artis brand affected by this recall?

    Yes, Artis products are affected by this recall. This recall involves Artis Zeego and Artis Zee medical systems sold in Canada. They are being recalled because software issues could block system movements. Healthcare professionals should stop using the affected products and follow the return/repair steps in the official notice.