ResMed recalls AirFit F30i Full Face Masks with potential magnetic interference affecting medical implants. Owners should check model numbers and follow safety guidelines.
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
ResMed is recalling AirFit F30i Full Face Masks due to magnets that could interfere with medical implants. This poses a risk for patients with certain implants or those in close contact with the mask.
The mask contains magnets that may interfere with active medical implants containing ferromagnetic material. This interference could cause malfunction or injury if the mask is used too close to such implants.
Patients using the mask or those in close physical contact with the mask are at risk if they have medical implants that interact with magnets. This includes individuals with pacemakers, neurostimulators, or other ferromagnetic implants.
Check for the AirFit F30i Full Face Mask with User Guide 638225/version 2020-02 or earlier. The product has specific UDI-DI/GTIN numbers listed in the recall notice.
Identify the mask model by checking the User Guide version and UDI-DI/GTIN numbers listed in the recall notice.
Reach out to ResMed directly for guidance on whether your mask is affected and next steps.
No, but you should check if your mask is affected and contact ResMed for specific guidance.
Medical implants that interact with magnets, such as pacemakers, neurostimulators, or other ferromagnetic implants.
Check the User Guide version (638225/version 2020-02 or earlier) and UDI-DI/GTIN numbers listed in the recall notice.
We’ve drafted a message you can send ResMed to request your refund or repair — edit it as you like.
Subject: Recall Z-0542-2024 — ResMed ResMed Hello, I own a ResMed that is covered by recall Z-0542-2024 from ResMed. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
