FDAAugust 26, 2022device

Philips BiPAP A40, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.

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

The hazard

Motor assemblies manufactured with nonconforming plastic that contributes to off-gassing of VOCs.

What to do

FDA enforcement status: Ongoing

Brands named

philips respironicsphilips

UPCs

606959042742606959042766606959042797606959067677606959067714606959042834606959067752606959067721606959068025

Recall history

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

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Philips BiPAP A40, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency. — Recall Details · AllClear