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Official recall record

F&P Airvo 3

Health Canada — Medical Devices · 2024-08-29 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2024-08-29
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

This recall relates to specific versions of software of the Airvo 3, and how the device responds when flow alignment alarm 3.2.2 occurs. When this happens in Airvo 3 devices set up with high pressure oxygen (HPO) and running software version 1.5.1 or earlier, the device will deliver room air only. If this happens, a patient may experience oxygen desaturation that could lead to hypoxia. Software version 1.5.2 updates the software algorithm and ensures the target therapy continues in the event that this alarm occurs. Recall Start Date: August 8, 2024

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 2026-05-31.

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