Medical devicesUpdated Jan 3, 2026Voco GmbhOfficial source

    Ionostar Plus and Ionolux recall in Canada: labelling and packaging issue

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    In plain language

    This recall involves Ionostar Plus and Ionolux dental products sold in Canada. They are being recalled due to incorrect plungers in some capsules, which can cause delayed or incomplete curing. Stop using the product and contact the manufacturer for more information.

    What to do

    • Stop using the product immediately.
    • Contact the manufacturer if you require additional information.

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    Affected products

    • Ionostar Plus

      Model: 2540, 2543, 2544, 2545, 2546, 2547, 2548, 2549

      Lot: More than 10 numbers, contact manufacturer.

    • Ionolux

      Model: 2115, 2117, 2118, 2119, 2120, 2121, 2122, 2123, 2124

      Lot: More than 10 numbers, contact manufacturer.

    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: More than 10 numbers, contact manufacturer.

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 2115, 2117, 2118, 2119, 2120, 2121, 2122, 2123, 2124, 2540, 2543, 2544, 2545, 2546, 2547, 2548, 2549

    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 Ionostar Plus and Ionolux dental products sold in Canada. They are being recalled due to incorrect plungers in some capsules, which can cause delayed or incomplete curing. Stop using the product and contact the manufacturer for more information.

    What should consumers do?

    Stop using the product immediately. Contact the manufacturer if you require 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?

    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 February 2, 2024.

    Is the Voco Gmbh brand affected by this recall?

    Yes, Voco Gmbh products are affected by this recall. This recall involves Ionostar Plus and Ionolux dental products sold in Canada. They are being recalled due to incorrect plungers in some capsules, which can cause delayed or incomplete curing. Stop using the product and contact the manufacturer for more information.