Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Quattro Air FFM MED AMER Recalled by Resmed Corporation Due to Masks in this lot, labelled and sold as...
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 Resmed Corporation directly.
Affected Products
Quattro Air FFM MED AMER, Product Code: 62702, full face mask for use with active-exhaust-valve ventilators
Quantity: 42 units
Why Was This Recalled?
Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size Medium actually contain a non-vented (NV) Quattro Air FFM Large mask.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Resmed Corporation
Resmed Corporation has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report