Official recall record
AirFit N10 Nasal Masks and User Guide
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2023-11-20
- Country of alert
- Australia
- Alert level
- Class I
- Alert type
- recall
- Barcode (EAN/GTIN)
- 619498632008
- Brand on record
- ResMed Ltd.
What the authority reported
Masks non-invasive interface for channeling airflow to patients have magnets that have potential magnetic interference with active medical implants that interact with magnets, and metallic implants/objects containing ferromagnetic material so contraindications and warnings about safe distance to medical devices/implants are being updated for patients using masks or anyone in close physical contact
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2023-11-20 · US FDA — Medical Devices
AirTouch F20 Full Face Mask and User Guide - 2023-11-20 · US FDA — Medical Devices
AirTouch N20 Nasal Mask and User Guide - 2023-11-20 · US FDA — Medical Devices
AirFit F30 Full Face Mask and User Guide
All 5 official recall notices naming ResMed Ltd. on this site →
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.