FDAAugust 26, 2022device

Philips BiPAP V30 Auto, 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

606959039377606959067936

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →