Official recall record
Airlife Adult Manual Resuscitator
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-04-05
- Country of alert
- Canada
- Alert level
- Type I
- Alert type
- recall
What the authority reported
Vyaire has received thirty-seven (37) customer reports relating to product issues, including two deaths and two serious injuries. It has been identified that the affected product issues are due to faulty mold/tooling producing out of specification components. This device failure may result in improper ventilation or no ventilation that may result in hypo-ventilation or hypoxia, and potentially may lead to death. Recall Start Date: January 10, 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.
Record last checked against the registry on 2026-05-31.
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