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Official recall record

Sevoflurane, Desflurane, and Isoflurane Electronic Vaporizer Material Package

Health Canada — Medical Devices · 2024-08-20 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2024-08-20
Last updated (per notice)
2024-11-15
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

The anesthesia system is a device used to administer a general inhalation anesthetic continuously or intermittently to a patient and maintain their ventilation. The A9 anesthesia system utilizes electronic vaporizers (V90) for anesthetic agent delivery. Mindray has become aware of a potential issue with select batches of V90 electronic vaporizers. The V90 electronic vaporizer anesthetic agent output may be higher than the set amount due to a component within the vaporizer causing an incomplete seal in some cases. Should this issue occur, the A9 anesthesia system will generate alarms associated with abnormal vaporizer output. We recommend that the user use the part number reference to identify the license and the device identifier. Recall start date: July 22, 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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ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.