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

    MAGNETOM MRI Systems recall in Canada: pressure build-up risk

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    In plain language

    This recall involves MAGNETOM MRI Systems (Prisma, Vida, Skyra, Verio, Lumina, Cima.X) and Biograph mMR System sold in Canada. They are being recalled because an ice blockage could cause pressure to build up in the system, potentially leading to a helium leak. Healthcare facilities should stop using the product and follow the return/repair steps in the official notice.

    What to do

    • ["Stop using the product immediately.","Contact the manufacturer for additional information.","Follow the manufacturer's instructions for inspection and repair."]

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    Affected products

    Specific affected products are listed in the official notice.

    Why this matters

    Pressure build-up and helium leak risk

    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?

    Pressure build-up and helium leak risk

    What should consumers do?

    ["Stop using the product immediately.","Contact the manufacturer for additional information.","Follow the manufacturer's instructions for inspection and repair."]

    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. Pressure build-up and helium leak risk

    When was this product recalled?

    This product was recalled on November 18, 2025.

    Is the Siemens Healthcare Gmbh brand affected by this recall?

    Yes, Siemens Healthcare Gmbh products are affected by this recall. This recall involves MAGNETOM MRI Systems (Prisma, Vida, Skyra, Verio, Lumina, Cima.X) and Biograph mMR System sold in Canada. They are being recalled because an ice blockage could cause pressure to build up in the system, potentially leading to a helium leak. Healthcare facilities should stop using the product and follow the return/repair steps in the official notice.