RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026Siemens Healthcare GmbhOfficial source

    Luminos, Uroskop, and Axiom Systems recall in Canada: collision risk

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    In plain language

    This recall involves Luminos, Uroskop, and Axiom medical imaging systems sold in Canada. They are being recalled because a software issue could cause the system to collide with the ceiling or wall during movement. Stop using the product and contact the manufacturer for more information.

    What to do

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

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    Affected products

    • Luminos Lotus Max

      Model: VF11C VF11G 11574100

    • Luminos Agile

      Model: VC10Q 10502200

    • Uroskop Omnia Max

      Model: VF11G VF10F VE10Z VF11C_HF01 10762473

    • Axiom Luminos Drf

      Model: VD10U VD10T 10094200

    • Luminos Drf Max

      Model: VF10F_HF03 VE10Y VF11C VF10F VF11E VF10C VF11C_HF01 10762471

    • Luminos Agile Max

      Model: 10762472

    • Uroskop Omnia

      Model: VD10U VD10P 10094910

    Why this matters

    Collision risk

    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 model number

      Model numbers are typically on the product label or packaging.

      Affected models: 10762472, VC10Q 10502200, VD10U VD10P 10094910, VD10U VD10T 10094200, VF10F_HF03 VE10Y VF11C VF10F VF11E VF10C VF11C_HF01 10762471, VF11C VF11G 11574100, VF11G VF10F VE10Z VF11C_HF01 10762473

    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?

    Collision risk

    What should consumers do?

    Stop using the product immediately. Contact the manufacturer for additional 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. Collision risk

    When was this product recalled?

    This product was recalled on February 24, 2023.

    Is the Siemens Healthcare Gmbh brand affected by this recall?

    Yes, Siemens Healthcare Gmbh products are affected by this recall. This recall involves Luminos, Uroskop, and Axiom medical imaging systems sold in Canada. They are being recalled because a software issue could cause the system to collide with the ceiling or wall during movement. Stop using the product and contact the manufacturer for more information.