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FDAFebruary 28, 2022device

Philips Respironics V680 Ventilator (All Models, including: P/N 1103044 (850011)), *Distributed outside the United States

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

The hazard

Ventilator units have an issue impacting an internal electrical circuit within the ventilators, that in some cases could result in the ventilator ceasing to operate.

What to do

FDA enforcement status: Ongoing

Brands named

respironics californiarespironics

Recall history

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

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