RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026MEDTRONIC INC.Official source

    Medtronic Crome and Cobalt MRI Surescan recall in Canada: performance issue

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    In plain language

    This recall involves Medtronic Crome and Cobalt MRI Surescan implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) sold in Canada. They are being recalled because of a potential for reduced shock energy during high-voltage therapy. Contact the manufacturer for additional information.

    What to do

    • Contact the manufacturer if you require additional information.

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    Affected products

    • Crome Hf Quad Crt-D Mri Surescan

      Model: DTPC2Q1, DTPC2QQ

      Lot: All lots

    • Crome Hf Crt-D Mri Surescan

      Model: DTPC2D1, DTPC2D4

      Lot: All lots

    • Crome Vr Mri Surescan

      Model: DVPC3D1, DVPC3D4

      Lot: All lots

    • Cobalt Hf Crt-D Mri Surescan

      Model: DTPB2D1, DTPB2D4

      Lot: All lots

    • Cobalt Dr Mri Surescan

      Model: DDPB3D1, DDPB3D4

      Lot: All lots

    • Crome Dr Mri Surescan

      Model: DDPC3D1, DDPC3D4

      Lot: All lots

    • Cobalt Xt Hf Crt-D Mri Surescan

      Model: DTPA2D1, DTPA2D4

      Lot: All lots

    • Cobalt Vr Mri Surescan

      Model: DVPB3D1, DVPB3D4

      Lot: All lots

    • Cobalt Hf Quad Crt-D Mri Surescan

      Model: DTPB2Q1, DTPB2QQ

      Lot: All lots

    Why this matters

    Performance 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: All lots

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: DDPB3D1, DDPB3D4, DDPC3D1, DDPC3D4, DTPA2D1, DTPA2D4, DTPB2D1, DTPB2D4, DTPB2Q1, DTPB2QQ, DTPC2D1, DTPC2D4, DTPC2Q1, DTPC2QQ, DVPB3D1, DVPB3D4, DVPC3D1, DVPC3D4

    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?

    Performance 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. Performance issue

    When was this product recalled?

    This product was recalled on July 4, 2022.

    Is the MEDTRONIC INC. brand affected by this recall?

    Yes, MEDTRONIC INC. products are affected by this recall. This recall involves Medtronic Crome and Cobalt MRI Surescan implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) sold in Canada. They are being recalled because of a potential for reduced shock energy during high-voltage therapy. Contact the manufacturer for additional information.