Official recall record
Volara System Patient Ciruit
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-05-29
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-06-10.
Record last checked against the registry on 2026-06-10.
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