RecallGuide.ca
    Health productsUpdated Feb 3, 2026OLYMPUS MEDICAL SYSTEMS CORP.Official source

    EVIS EXERA III Duodenovideoscope

    Share:

    In plain language

    This recall involves the OLYMPUS MEDICAL SYSTEMS CORP. EVIS EXERA III Duodenovideoscope. It's being recalled because of updated labelling and packaging information. Users should review the updated materials and follow the instructions.

    What to do

    • Review the updated reprocessing materials.
    • Follow the operation and reprocessing instructions.
    • Contact the manufacturer for more information.

    Get alerts for recalls like this

    Get email alerts when new recalls affect products in this category.

    Categories (optional)

    No spam. Unsubscribe anytime. We only email when there's a relevant recall.

    Affected products

    • EVIS EXERA III Duodenovideoscope

      Model: TJF-Q190V

      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: TJF-Q190V

    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 OLYMPUS MEDICAL SYSTEMS CORP. EVIS EXERA III Duodenovideoscope. It's being recalled because of updated labelling and packaging information. Users should review the updated materials and follow the instructions.

    What should consumers do?

    Review the updated reprocessing materials. Follow the operation and reprocessing instructions. Contact the manufacturer for more 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 February 3, 2026.

    Is the OLYMPUS MEDICAL SYSTEMS CORP. brand affected by this recall?

    Yes, OLYMPUS MEDICAL SYSTEMS CORP. products are affected by this recall. This recall involves the OLYMPUS MEDICAL SYSTEMS CORP. EVIS EXERA III Duodenovideoscope. It's being recalled because of updated labelling and packaging information. Users should review the updated materials and follow the instructions.