Medical devicesUpdated Jan 3, 2026BLUSelect®, BLUgriggs®, BLUperc®Official source

    BLUSelect®, BLUgriggs® and BLUperc® Products

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    In plain language

    This recall involves BLUSelect®, BLUgriggs®, and BLUperc® tracheostomy products sold in Canada. They are being recalled because of a manufacturing defect that may cause the pilot balloon to disconnect. Stop using the product and contact the manufacturer for more information.

    What to do

    • Stop using the product immediately.
    • Contact the manufacturer for additional information.

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    Affected products

    • BLUgriggs Percutaneous Dilation Tracheostomy Kit

      Model: 101/541/080

      Lot: More than 10 numbers, contact manufacturer.

    • BLUperc Percutaneous Dilation Tracheostomy Kit

      Model: 101/561/070, 101/561/080, 101/561/090, 101/563/070, 101/563/080

      Lot: More than 10 numbers, contact manufacturer.

    • BLUSelect Tracheostomy Tubes

      Model: 101/815/060, 101/815/070, 101/815/075, 101/815/080, 101/815/085, 101/815/090, 101/815/100, 101/817/060, 101/817/070, 101/817/080, 101/817/090, 101/875/060, 101/875/070, 101/875/075, 101/875/080, 101/875/085, 101/875/090

      Lot: More than 10 numbers, contact manufacturer.

    Why this matters

    Performance issue due to manufacturing defect

    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: 101/541/080, 101/561/070, 101/561/080, 101/561/090, 101/563/070, 101/563/080, 101/815/060, 101/815/070, 101/815/075, 101/815/080, 101/815/085, 101/815/090, 101/815/100, 101/817/060, 101/817/070, 101/817/080, 101/817/090, 101/875/060, 101/875/070, 101/875/075, 101/875/080, 101/875/085, 101/875/090

    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?

    Performance issue due to manufacturing defect

    What should consumers do?

    Stop using the product immediately. Contact the manufacturer 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?

    Yes, there may be a health risk. Performance issue due to manufacturing defect

    When was this product recalled?

    This product was recalled on June 10, 2024.

    Is the BLUSelect®, BLUgriggs®, BLUperc® brand affected by this recall?

    Yes, BLUSelect®, BLUgriggs®, BLUperc® products are affected by this recall. This recall involves BLUSelect®, BLUgriggs®, and BLUperc® tracheostomy products sold in Canada. They are being recalled because of a manufacturing defect that may cause the pilot balloon to disconnect. Stop using the product and contact the manufacturer for more information.