Medical devicesUpdated Jan 3, 2026Oridion MedicalOfficial source

    Oridion Medical recall in Canada: Medical device labelling and packaging issue

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    This recall involves various Oridion Medical Filterline, Vitaline H sets, Airway Adapters, Ventline Set, and CO2 Sampling Lines sold in Canada. It's being recalled because of issues with labelling and packaging, specifically difficulty disconnecting the airway adapter. Stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Contact the manufacturer, Oridion Medical 1987 Ltd., for additional information.

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    Affected products

    • Filterline Set

      Model: XS04620

      Lot: All lots.

    • Filterline H Set Infant/Neonatal

      Model: 006324

      Lot: All lots.

    • Omni Ventline Set

      Model: 012495

      Lot: All lots.

    • Filterline H Set

      Model: XS04624

      Lot: All lots.

    • Filterline H Set Adult/Pediatric

      Model: 007737 010580

      Lot: All lots.

    • Airway Adapter, Adult/Pediatric

      Model: 010989

      Lot: All lots.

    • CO2 Sampling Line

      Model: 010991

      Lot: All lots.

    • Filterline H Set Infant/Neonatal, Long

      Model: 007738

      Lot: All lots.

    • Filterline Set Long, Adult/Pediatric

      Model: 010579 007768

      Lot: All lots.

    • Vitaline H Set Adult/Pediatric

      Model: 010787

      Lot: All lots.

    • Vitaline H Set Infant/Neonatal

      Model: 010807

      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: 006324, 007737 010580, 007738, 010579 007768, 010787, 010807, 010989, 010991, 012495, XS04620, XS04624

    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 various Oridion Medical Filterline, Vitaline H sets, Airway Adapters, Ventline Set, and CO2 Sampling Lines sold in Canada. It's being recalled because of issues with labelling and packaging, specifically difficulty disconnecting the airway adapter. Stop using the product and follow the return/repair steps in the official notice.

    What should consumers do?

    Stop using the product immediately. Contact the manufacturer, Oridion Medical 1987 Ltd., 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 6, 2025.

    Is the Oridion Medical brand affected by this recall?

    Yes, Oridion Medical products are affected by this recall. This recall involves various Oridion Medical Filterline, Vitaline H sets, Airway Adapters, Ventline Set, and CO2 Sampling Lines sold in Canada. It's being recalled because of issues with labelling and packaging, specifically difficulty disconnecting the airway adapter. Stop using the product and follow the return/repair steps in the official notice.