
Vyaire Medical Recalls AirLife Humidification Chamber & Heated Breathing Circuit Kits Due to Manufacturing Error
The U.S. Food & Drug Administration (FDA) has issued a Class I recall of Vyaire’s AirLife Humidification Chamber & Heated Breathing Circuit Kits due to manufacturing errors. Class I recalls are the FDA’s most serious type of recalls. The FDA notes that the use of these products can cause serious injury or death. Recalled Product(s): Air Life … Read more