SafeRecalls
Back to search

🇨🇦 Celon ProBreath and Celon ProSleep Applicators

Recall date: February 20, 2026Country: CACategory: medical_devices
Hazard/Reason: 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.
This page links to official sources. Verify model/lot/batch details in the official notice.