Celon ProBreath and Celon ProSleep Applicators
In plain language
This recall involves Olympus Celon ProBreath and Celon ProSleep applicators sold in Canada. They are being recalled because some boxes were shipped without the required Instructions For Use (IFU). Users should get the IFU from Olympus Canada and keep a copy with the device.
What to do
- Contact Olympus Canada Technical Assistance Center (TAC) to obtain the Instructions For Use (IFU).
- Ensure a copy of the IFU is placed with the device.
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Affected products
Celon ProSleep Plus Bipolar Applicator
Model: WB990008
Lot: 1000169653
Celon ProSleep Plus
Model: WB990095
Lot: 1000169656
Celon ProBreath Bipolar Applicator
Model: WB990007
Lot: 1000169475, 1000171773, 1000172947, 1000172948, 1000172949
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: 1000169475, 1000169653, 1000169656, 1000171773, 1000172947, 1000172948, 1000172949
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: WB990007, WB990008, WB990095
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.
Frequently Asked Questions
Why was this product recalled?
This recall involves Olympus Celon ProBreath and Celon ProSleep applicators sold in Canada. They are being recalled because some boxes were shipped without the required Instructions For Use (IFU). Users should get the IFU from Olympus Canada and keep a copy with the device.
What should consumers do?
Contact Olympus Canada Technical Assistance Center (TAC) to obtain the Instructions For Use (IFU). Ensure a copy of the IFU is placed with the device.
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 20, 2026.
Is the Olympus brand affected by this recall?
Yes, Olympus products are affected by this recall. This recall involves Olympus Celon ProBreath and Celon ProSleep applicators sold in Canada. They are being recalled because some boxes were shipped without the required Instructions For Use (IFU). Users should get the IFU from Olympus Canada and keep a copy with the device.