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🇨🇦 Volara System Patient Ciruit

Recall date: May 29, 2026Country: CACategory: medical_devices
Hazard/Reason: Baxter Corporation is issuing an urgent medical device correction for Volara System patient circuits due to reports of air and medication leakage from the nebulizer cup during therapy. The leakage can lead to patient desaturation and ineffective nebulization, impacting the delivery of prescribed therapy.  
This page links to official sources. Verify model/lot/batch details in the official notice.