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FDAJune 30, 2025device

DreamStation Auto BiPAP. Non-Continuous Ventilator.

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

The hazard

Devices may possess a programming error resulting in an incorrect device configuration.

What to do

FDA enforcement status: Ongoing

Brands named

philips respironicsphilips

UPCs

606959429772

Recall history

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

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DreamStation Auto BiPAP. Non-Continuous Ventilator. — Recall Details · AllClear