FDAMay 9, 2025device

BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients weighing over 10 kg.

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

The hazard

This device does not indicate for use in patients with respiratory failure.

What to do

FDA enforcement status: Ongoing

Brands named

philips respironicsphilips

UPCs

0060959049635

Recall history

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

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BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients weighing over 10 kg. — Recall Details · AllClear