RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026Synchro 2Official source

    Synchro 2 Guidewire recall in Canada: Incorrect label information

    Share:

    In plain language

    This recall involves Synchro 2/Guidewire (Soft, Standard) products sold in Canada. It's being recalled because the product labels have an incorrect value for the Guidewire Outer Diameter dimension. The inches dimension on the label is correct.

    What to do

    • Stop using the product immediately.
    • Check model numbers M00326010, M00326310, M00326410, and M00326510.
    • Contact Stryker Neurovascular for more information.

    Get alerts for recalls like this

    Get email alerts when new recalls affect products in this category.

    Categories (optional)

    No spam. Unsubscribe anytime. We only email when there's a relevant recall.

    Affected products

    • Synchro 2/ Soft Guidewire

      Model: M00326010, M00326310

      Lot: More than 10 numbers, contact manufacturer.

    • Synchro 2/ Standard Guidewire

      Model: M00326410, M00326510

      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: M00326010, M00326310, M00326410, M00326510

    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.

    Want alerts if similar products are recalled in Canada?

    Frequently Asked Questions

    Why was this product recalled?

    This recall involves Synchro 2/Guidewire (Soft, Standard) products sold in Canada. It's being recalled because the product labels have an incorrect value for the Guidewire Outer Diameter dimension. The inches dimension on the label is correct.

    What should consumers do?

    Stop using the product immediately. Check model numbers M00326010, M00326310, M00326410, and M00326510. Contact Stryker Neurovascular for more 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 March 15, 2019.

    Is the Synchro 2 brand affected by this recall?

    Yes, Synchro 2 products are affected by this recall. This recall involves Synchro 2/Guidewire (Soft, Standard) products sold in Canada. It's being recalled because the product labels have an incorrect value for the Guidewire Outer Diameter dimension. The inches dimension on the label is correct.