Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Airvo 2 Humidifier Recalled by Fisher & Paykel Healthcare, Ltd. Due to Humidifier devices, used to deliver high flow respiratory...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Fisher & Paykel Healthcare, Ltd. directly.
Affected Products
Airvo 2 Humidifier, REF: PT101US, and myAirvo 2 Humidifier, REF: PT100US
Quantity: 7,147
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Fisher & Paykel Healthcare, Ltd.
Fisher & Paykel Healthcare, Ltd. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report