RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026Elekta Solutions AbOfficial source

    Elekta Modulator Discharge Rod recall in Canada: Performance issue

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    In plain language

    This recall involves Elekta Modulator Discharge Rods used in medical devices sold in Canada. They are being recalled because a manufacturing defect could affect their performance. Healthcare professionals should stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Elekta will contact users to check and replace faulty discharge rod crimps.

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    Affected products

    • Elekta Infinity

      Model: 1550358, 1552092

      Lot: All lots

    • Versa HD

      Model: 1550359, 1552093

      Lot: All lots

    • Harmony

      Model: 1553032

      Lot: All lots

    • Elekta Synergy

      Model: 1550291, 1550357

      Lot: All lots

    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: All lots

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 1550291, 1550357, 1550358, 1550359, 1552092, 1552093, 1553032

    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 Elekta Modulator Discharge Rods used in medical devices sold in Canada. They are being recalled because a manufacturing defect could affect their performance. Healthcare professionals should stop using the product and follow the return/repair steps in the official notice.

    What should consumers do?

    Stop using the product immediately. Elekta will contact users to check and replace faulty discharge rod crimps.

    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 November 19, 2025.

    Is the Elekta Solutions Ab brand affected by this recall?

    Yes, Elekta Solutions Ab products are affected by this recall. This recall involves Elekta Modulator Discharge Rods used in medical devices sold in Canada. They are being recalled because a manufacturing defect could affect their performance. Healthcare professionals should stop using the product and follow the return/repair steps in the official notice.