RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026Official source

    Hex Driver, 2.5/110mm AO recall in Canada: epoxy migration

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    In plain language

    This recall involves the Hex Driver, 2.5/110mm AO, sold in Canada. It's being recalled because the epoxy color band can migrate onto the shaft or sterilization tray after sterilization. Stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Check model and lot numbers.
    • Return, repair, or dispose of it as instructed.

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    Affected products

    • Hex Driver, 2.5/110mm AO

      Model: HXDRIVR-2.5AO

      Lot: 91956, 91957, 92237, 92238

    Why this matters

    Epoxy migration

    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: 91956, 91957, 92237, 92238

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: HXDRIVR-2.5AO

    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?

    Epoxy migration

    What should consumers do?

    Stop using the product immediately. Check model and lot numbers. Return, repair, or dispose of it as instructed.

    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. Epoxy migration

    When was this product recalled?

    This product was recalled on November 28, 2018.