FDAAugust 26, 2022device

Philips OmniLab Advanced+ Intl (Flow Gen), 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

606959029415606959028791

Recall history

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

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