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Airlife adult manual resuscitator
Official notice
5 Apr 2024
Last checked
5 Apr 2024
An official Health Canada notice concerns Airlife adult manual resuscitator. 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 Published 2024-04-05.
What to do now
Contact the manufacturer if you require additional information.
Recall number
75349
Official notice
2024-04-05
The hazard
The hazard
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
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Vyaire Medical, Airlife Adult Manual Resuscitator.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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