FDAMay 9, 2025device

BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support in adult and pediatric patients weighing more than 10 kg. BiPAP Hybrid A30 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients.

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

The hazard

This device does not indicate for use in patients with respiratory failure.

What to do

FDA enforcement status: Ongoing

Brands named

philips respironicsphilips

UPCs

006069590215320060695903930800606959039315006069590393390060695903934600606959039353006069590393600060695903938400606959039391006069590427280060695904874400606959048751

Recall history

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

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