RecallGuide.ca
    Medical devicesUpdated Mar 5, 2026OlympusOfficial source

    Olympus valve recall in Canada: Reprocessing issue

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    In plain language

    This recall involves Olympus MAJ-1443 and MAJ-1444 valves sold in Canada. They are being recalled because they are no longer compatible with certain automated endoscope reprocessors. Healthcare facilities must use updated reprocessing methods for these valves.

    What to do

    • Stop using the OER-Pro or OER-Elite automated reprocessors for these valves.
    • Refer to the updated instructions for use (IFU) for reprocessing methods.
    • Contact Olympus for additional information.

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    Affected products

    • Air/Water Valves

      Model: MAJ-1444

      Lot: All lots

    • Reusable Suction Valve

      Model: MAJ-1443

      Lot: All lots

    • Endoscope Reprocessor

      Model: OER-ELITE, OER-PRO

      Lot: All lots

    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: MAJ-1443, MAJ-1444, OER-ELITE, OER-PRO

    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?

    This recall involves Olympus MAJ-1443 and MAJ-1444 valves sold in Canada. They are being recalled because they are no longer compatible with certain automated endoscope reprocessors. Healthcare facilities must use updated reprocessing methods for these valves.

    What should consumers do?

    Stop using the OER-Pro or OER-Elite automated reprocessors for these valves. Refer to the updated instructions for use (IFU) for reprocessing methods. Contact Olympus for 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?

    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 5, 2026.

    Is the Olympus brand affected by this recall?

    Yes, Olympus products are affected by this recall. This recall involves Olympus MAJ-1443 and MAJ-1444 valves sold in Canada. They are being recalled because they are no longer compatible with certain automated endoscope reprocessors. Healthcare facilities must use updated reprocessing methods for these valves.