ResMed recalls AirFit F30 Full Face Masks with potential magnetic interference for patients with medical implants. Affected masks include specific model versions and lots sold since 2020.
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 F30 Full Face Masks that could interfere with medical implants due to magnets. This risk is serious for people with certain medical devices, as the masks might cause harm if used too close to implants.
The mask contains magnets that could interfere with active medical implants containing ferromagnetic material. This interference might cause malfunction or injury if the mask is used too close to the implant, especially during normal use.
Patients using the AirFit F30 mask with medical implants or those in close contact with such implants are most at risk. Anyone with a medical device that interacts with magnets should avoid using the mask without consulting a healthcare provider.
Check for the AirFit F30 Full Face Mask with User Guide version 2020-07 or earlier. Affected units have specific UDI-DI/GTIN numbers listed in the recall notice.
Look for the User Guide version number on the mask packaging or included materials; affected models have version 2020-07 or earlier.
If you have a medical implant that interacts with magnets, contact your healthcare provider before using the mask to ensure safety.
The recall applies to all users, but the risk is primarily for those with medical implants. If you don't have implants, the risk is low, but you should check the mask version.
The recall does not specify a return or replacement process. You should check with ResMed directly for guidance on safe use or alternatives.
Yes, affected masks include specific UDI-DI/GTIN numbers listed in the recall notice, such as 619498641048 and 619498641000.
We’ve drafted a message you can send ResMed to request your refund or repair — edit it as you like.
Subject: Recall Z-0541-2024 — ResMed ResMed Hello, I own a ResMed that is covered by recall Z-0541-2024 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.
