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🇨🇦 Fluoroplastic Vent Tube

Recall date: October 6, 2026Country: CACategory: medical_devices
Hazard/Reason: Vent tube devices across lot 0231048280 were identified to have been released to customers without undergoing sterilization. the issue is currently understood to originate from manufacturing (load preparation) and represents a fault condition: the product does not meet its specification for sterility (SAL 10-6) or its labeled sterile state.
This page links to official sources. Verify model/lot/batch details in the official notice.