Vyaire Medical Recalls AirLife Manual Resuscitators
The Class I recall of certain AirLife manual resuscitators is due to a manufacturing defect that may prevent patients from receiving enough ventilation, which could lead to injury or death.
The Class I recall of certain AirLife manual resuscitators is due to a manufacturing defect that may prevent patients from receiving enough ventilation, which could lead to injury or death.
Vyaire Medical's new AirLife Open oxygen mask provides the benefits of traditional cannula, mask and non-rebreather devices into a single solution.
Vyaire Medical Inc will now be the exclusive distributor of the Fenom Pro Asthma Monitor, a fractional exhaled nitric oxide (FeNO) device manufactured by Spirosure Inc.
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