FDAMay 8, 2018device

AirLife Resuscitation Device, Adult labeled as the following: a. Adult, with mask, oxygen reservoir bag, Part Number 2K8004; b. Adult, with mask, oxygen reservoir bag, CO2 detector, PEEP valve, Part Number 2K8035C2; c. Adult, with mask, 28" large bore tubing, Part Number 2K8017; d. Adult, with ma...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

An error in manufacturing of the AirLife Resuscitation Devices that has the potential to obstruct airflow of the supplemental oxygen delivery during use.

What to do

FDA enforcement status: Terminated

Brands named

vyaire medicalvyaire

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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