RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026HydroMARKOfficial source

    HydroMARK Breast Biopsy Marker recall in Canada: incorrect labeling

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    In plain language

    This recall involves the HydroMARK Breast Biopsy Marker sold in Canada. It's being recalled because of incorrect labeling on the packaging regarding the compatible introducer needle size. Stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Check the lot number on your product.
    • Contact Devicor Medical Products, Inc. for further instructions.

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    Affected products

    • HydroMARK Breast Biopsy Marker

      Model: 4010-02-18-T3

      Lot: 200044757, 200045089, 200045387, 200045531, 200045553, 200045745, 200045916

    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: 200044757, 200045089, 200045387, 200045531, 200045553, 200045745, 200045916

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 4010-02-18-T3

    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 the HydroMARK Breast Biopsy Marker sold in Canada. It's being recalled because of incorrect labeling on the packaging regarding the compatible introducer needle size. Stop using the product and follow the return/repair steps in the official notice.

    What should consumers do?

    Stop using the product immediately. Check the lot number on your product. Contact Devicor Medical Products, Inc. for further instructions.

    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 October 19, 2018.

    Is the HydroMARK brand affected by this recall?

    Yes, HydroMARK products are affected by this recall. This recall involves the HydroMARK Breast Biopsy Marker sold in Canada. It's being recalled because of incorrect labeling on the packaging regarding the compatible introducer needle size. Stop using the product and follow the return/repair steps in the official notice.