Recall Monitor
Health Products

Celon ProBreath and Celon ProSleep Applicators

· Published by Health Canada · Official notice

Details

Alert type: Health product recall
Category: Health products - Medical devices - General and plastic surgery
Product: Celon ProBreath and Celon ProSleep Applicators
Issue: Medical devices - Labelling and packaging
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare
Recall class: Type II
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Products

Affected productsLot or serial numberModel or catalogue number
Celon ProSleep Plus Bipolar Applicator1000169653WB990008
Celon ProSleep Plus1000169656WB990095
Celon ProBreath Bipolar Applicator1000172949WB990007
Celon ProBreath Bipolar Applicator1000172947WB990007
Celon ProBreath Bipolar Applicator1000171773WB990007
Celon ProBreath Bipolar Applicator1000172948WB990007
Celon ProBreath Bipolar Applicator1000169475WB990007

Issue

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.

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