Medical devicesUpdated Jan 3, 2026St. Jude Medical, Cardiac Rhythm Management DivisionOfficial source

    Assurity and Endurity Pacemakers recall in Canada: device malfunction

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    In plain language

    This recall involves Assurity and Endurity Pacemakers sold in Canada. They are being recalled because a manufacturing issue may cause the device to malfunction. Contact the manufacturer for more information.

    What to do

    • Contact the manufacturer if you require additional information.

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    Affected products

    • Assurity Pulse Generator

      Model: PM2240

      Lot: More than 10 numbers, contact manufacturer.

    • Assurity MRI Pacemaker

      Model: PM1272 PM2272

      Lot: More than 10 numbers, contact manufacturer.

    • Endurity Pulse Generator

      Model: PM1160

      Lot: More than 10 numbers, contact manufacturer.

    • Endurity MRI Pacemaker

      Model: PM1172 PM2172

      Lot: More than 10 numbers, contact manufacturer.

    Why this matters

    Device malfunction

    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: PM1160, PM1172 PM2172, PM1272 PM2272, PM2240

    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?

    Device malfunction

    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. Device malfunction

    When was this product recalled?

    This product was recalled on February 27, 2025.

    Is the St. Jude Medical, Cardiac Rhythm Management Division brand affected by this recall?

    Yes, St. Jude Medical, Cardiac Rhythm Management Division products are affected by this recall. This recall involves Assurity and Endurity Pacemakers sold in Canada. They are being recalled because a manufacturing issue may cause the device to malfunction. Contact the manufacturer for more information.