FDAApril 2, 2024device

Airvo 2 Humidifier, REF: PT101US, and myAirvo 2 Humidifier, REF: PT100US

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

The hazard

Humidifier devices, used to deliver high flow respiratory therapy to patients, manufactured before 14 August 2017, have a speaker configuration that may result in distorted, intermittent or inaudible alarm sound levels. In the absence of an audible alarm, if there is an interruption to therapy, a patient may experience oxygen desaturation.

What to do

FDA enforcement status: Ongoing

Brands named

fisher paykel healthcarefisherfisher paykel

UPCs

0942001242224809420012422347

Recall history

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

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