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Celon probreath and celon prosleep applicators

Official notice

20 Feb 2026

Last checked

20 Feb 2026

Medium riskHealth Canada
Watch Olympus Winter Ibe

An official Health Canada notice concerns Celon probreath and celon prosleep applicators. Olympus has identified that certain boxes of Celon ProBreath and Celon ProSleep Plus bipolar applicators were released to customers without the required Instructions For Use (IFU) included. Users should obtain the IFU through Olympus Canada Technical Assistance Center (TAC) and ensure a copy of the IFU is placed with the device. Published 2026-02-20.

What to do now

Contact the manufacturer if you require additional information.

Recall number

81630

Official notice

2026-02-20

The hazard

Olympus has identified that certain boxes of Celon ProBreath and Celon ProSleep Plus bipolar applicators were released to customers without the required Instructions For Use (IFU) included. Users should obtain the IFU through Olympus Canada Technical Assistance Center (TAC) and ensure a copy of the IFU is placed with the device.

How to check if you're affected

Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.

Lots

1000169653, 1000169656, 1000172949, 1000172947, 1000171773, 1000172948, 1000169475

Skus

WB990008, WB990095, WB990007

Other

RA RA-81630

Model Numbers

WB990008, WB990095, WB990007

Recall Numbers

81630

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Affected products

Product 1

Lot or serial number - 1000169653, Model or catalogue number - WB990008

Product 2

Lot or serial number - 1000169656, Model or catalogue number - WB990095

Product 3

Lot or serial number - 1000172949, Model or catalogue number - WB990007

Product 4

Lot or serial number - 1000172947, Model or catalogue number - WB990007

Product 5

Lot or serial number - 1000171773, Model or catalogue number - WB990007

Product 6

Lot or serial number - 1000172948, Model or catalogue number - WB990007

Product 7

Lot or serial number - 1000169475, Model or catalogue number - WB990007

Risk / hazard

Olympus has identified that certain boxes of Celon ProBreath and Celon ProSleep Plus bipolar applicators were released to customers without the required Instructions For Use (IFU) included. Users should obtain the IFU through Olympus Canada Technical Assistance Center (TAC) and ensure a copy of the IFU is placed with the device.

Where it was sold

The source does not list specific retailers. See the official notice for where affected vehicles were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Brand

Olympus Winter Ibe

Manufacturer

Not provided

Phone

Not provided

Brand: Olympus Winter Ibe.

Source & status

Source

Health Canada

Tier

official

Category

HOME

Classification

Type II

App estimate

medium

Recall details

Recall number

81630

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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