FDAAugust 26, 2022device

Philips BiPAP A30, 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

606959042667606959042681606959042698606959042728606959067585606959067530

Recall history

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

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