RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026TrueBeamOfficial source

    TrueBeam, TrueBeam STx, and TrueBeam Edge recall in Canada: unintended override

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    In plain language

    This recall involves TrueBeam, TrueBeam STx, and TrueBeam Edge medical devices sold in Canada. They are being recalled because of an unintended override of gated treatment plans. Stop using the product and follow the return steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Check model and serial numbers.
    • Follow the instructions from your healthcare provider or the manufacturer.

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    Affected products

    • TrueBeam

      Model: Versions 2.0, Versions 2.5

    • TrueBeam STx

      Model: Versions 2.0, Versions 2.5

    • TrueBeam Edge

      Model: Versions 2.0, Versions 2.5

    Why this matters

    Unintended override of gated treatment plan

    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: Versions 2.0, Versions 2.5

    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?

    Unintended override of gated treatment plan

    What should consumers do?

    Stop using the product immediately. Check model and serial numbers. Follow the instructions from your healthcare provider or the manufacturer.

    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. Unintended override of gated treatment plan

    When was this product recalled?

    This product was recalled on September 7, 2018.

    Is the TrueBeam brand affected by this recall?

    Yes, TrueBeam products are affected by this recall. This recall involves TrueBeam, TrueBeam STx, and TrueBeam Edge medical devices sold in Canada. They are being recalled because of an unintended override of gated treatment plans. Stop using the product and follow the return steps in the official notice.