FDAMarch 26, 2024device

BiPAP V30 Auto Ventilator, Part Number 1111178

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

The hazard

Potential for devices to experience interruption/loss of therapy during a Ventilator Inoperative alarm. This may lead to hypoventilation, mild to severe hypoxemia, hypercarbia, respiratory failure/insufficiency, or potentially death in the most vulnerable patients.

What to do

FDA enforcement status: Ongoing

Brands named

philips respironicsphilips

UPCs

00606959049635

Recall history

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

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