RecallGuide.ca
    Health productsUpdated Jan 3, 2026Inderal-LAOfficial source

    Inderal-LA recall in Canada: nitrosamine impurity

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    In plain language

    This recall involves Inderal-LA (propranolol hydrochloride) extended release capsules sold in Canada. It's being recalled because of a nitrosamine impurity (N-nitroso-propranolol) above acceptable levels. Continue taking your medication unless advised otherwise by your healthcare provider, and contact them to discuss other treatment options.

    What to do

    • Contact your healthcare provider to discuss other treatment options.
    • Continue taking your medication unless advised to stop by your healthcare provider.
    • Contact Pfizer Canada ULC for medical inquiries at 1-800-463-6001 or general inquiries at 1-800-387-4974.
    • Report any health product-related side effects or complaints to Health Canada.

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    Affected products

    • Inderal-LA 60 mg

      Lot: DX6150, EH5907, EX7461

      Date codes: 2023-03-31, 2023-08-31, 2024-01-31

    • Inderal-LA 80 mg

      Lot: DJ2768, DW8242, EE7221, EL1695, EX7462

      Date codes: 2022-09-30, 2023-03-31, 2023-05-31, 2023-08-31, 2024-01-31

    • Inderal-LA 120 mg

      Lot: DJ6820, DX6159, EH5908, FE0541

      Date codes: 2022-09-30, 2023-03-31, 2023-08-31, 2024-01-31

    • Inderal-LA 160 mg

      Lot: DW8241, EH5906, FE6304

      Date codes: 2023-03-31, 2023-08-31, 2024-01-31

    Why this matters

    Increased cancer risk from long-term exposure

    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 date code

      Date codes are usually printed near the best-before date or on the packaging seam.

      Affected date codes: 2022-09-30, 2023-03-31, 2023-05-31, 2023-08-31, 2024-01-31

    3. 3

      Check the lot number

      Lot numbers identify specific production batches.

      Affected lots: DJ2768, DJ6820, DW8241, DW8242, DX6150, DX6159, EE7221, EH5906, EH5907, EH5908, EL1695, EX7461, EX7462, FE0541, FE6304

    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?

    Increased cancer risk from long-term exposure

    What should consumers do?

    Contact your healthcare provider to discuss other treatment options. Continue taking your medication unless advised to stop by your healthcare provider. Contact Pfizer Canada ULC for medical inquiries at 1-800-463-6001 or general inquiries at 1-800-387-4974. Report any health product-related side effects or complaints to Health Canada.

    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. Increased cancer risk from long-term exposure

    When was this product recalled?

    This product was recalled on March 1, 2022.

    Is the Inderal-LA brand affected by this recall?

    Yes, Inderal-LA products are affected by this recall. This recall involves Inderal-LA (propranolol hydrochloride) extended release capsules sold in Canada. It's being recalled because of a nitrosamine impurity (N-nitroso-propranolol) above acceptable levels. Continue taking your medication unless advised otherwise by your healthcare provider, and contact them to discuss other treatment options.