FDAMay 8, 2018device

AirLife Resuscitation Device, Pediatric labeled as the following: a. Pediatric, with mask, 28" large bore tubing, pressure-relief valve, Part Number 2K8018; b. Pediatric, with mask, 40" oxygen reservoir bag, pressure-relief valve, Part Number 2K8008; c. Pediatric, Resuscitation kit with neonatal,...

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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