FDAJanuary 10, 2024device

AirLife Adult Manual Resuscitator, 40" (1.0m) Oxygen Reservoir Tubing, Adult Mask, Expiratory Filter, REF 2K8005F

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

The hazard

Risk of hypoventilation caused by duckbill and ring broken/disassembled, due to faulty mold/tooling producing out of specification components. Device failure may cause improper ventilation or no ventilation that may result in hypoventilation or hypoxia, and potentially lead to death. The mold/tooling used to produce the affected component was replaced in 2017.

What to do

FDA enforcement status: Ongoing

Brands named

vyaire medicalvyaire

UPCs

5019075211418810190752114180

Recall history

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

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