FDAMay 9, 2025device

BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients. BiPAP A40 Pro - sold OUS

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

00606959039476

Recall history

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

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