Medical devicesUpdated Jan 3, 2026Olympus Winter & Ibe GmbHOfficial source

    OES Pro Urology Resection Sheaths recall in Canada: device compatibility

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    In plain language

    This recall involves OES Pro Urology Resection Sheaths sold in Canada. They are being recalled because of device compatibility issues with a specific laser. Healthcare professionals should contact the manufacturer for more information.

    What to do

    • Contact the manufacturer if you require additional information.

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    Affected products

    • OES Pro Urology Resection Sheaths

      Model: WA22810A

      Lot: More than 10 numbers, contact manufacturer.

    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: WA22810A

    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 OES Pro Urology Resection Sheaths sold in Canada. They are being recalled because of device compatibility issues with a specific laser. Healthcare professionals should contact the manufacturer for more information.

    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?

    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 October 30, 2024.

    Is the Olympus Winter & Ibe GmbH brand affected by this recall?

    Yes, Olympus Winter & Ibe GmbH products are affected by this recall. This recall involves OES Pro Urology Resection Sheaths sold in Canada. They are being recalled because of device compatibility issues with a specific laser. Healthcare professionals should contact the manufacturer for more information.