Medical devicesUpdated Jan 3, 2026Stryker InstrumentsOfficial source

    TPS System – Elite Burs recall in Canada: Sterility issue

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    In plain language

    This recall involves TPS System – Elite Burs sold in Canada. It's being recalled because the devices may not be sterile. Contact the manufacturer for more information.

    What to do

    • Contact the manufacturer if you require additional information.

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    Affected products

    • TPS System – Elite Burs

      Model: 5820-066-012

      Lot: 22329017

    Why this matters

    Sterility issue

    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: 22329017

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 5820-066-012

    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?

    Sterility issue

    What should consumers do?

    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?

    Yes, there may be a health risk. Sterility issue

    When was this product recalled?

    This product was recalled on September 24, 2024.

    Is the Stryker Instruments brand affected by this recall?

    Yes, Stryker Instruments products are affected by this recall. This recall involves TPS System – Elite Burs sold in Canada. It's being recalled because the devices may not be sterile. Contact the manufacturer for more information.