FDAApril 1, 2024device

OmniLab Advanced + Ventilator Product Numbers 1111122 1111123 1111124 1111125 1111126 1111127 1111138 1111141 1111142 KR1111127 R1111122 R1111123 R1111124 U1111122 U1111124

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

The hazard

Device may experience an interruption or loss of therapy in case of a Ventilator Inoperative alarm. This may lead to hypoventilation, mild to severe hypoxemia, hypercarbia, respiratory failure/insufficiency, or potentially death.

What to do

FDA enforcement status: Ongoing

Brands named

philips respironicsphilips

UPCs

606959067813606959067820606959067837

Recall history

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

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