AIRFIT F20Recalls & reported problems across all models
Resmed Pty Ltd · 12 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one AIRFIT F20 model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 12 models of AIRFIT F20 by Resmed Pty Ltd in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
AIRFIT F20 recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Nov 20, 2023Class IOpen, Classified
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
Z-0537-2024 · Root cause: Device Design · names 12 of these models · Recall details · FDA record ↗
AIRFIT F20 models
12 models, most reported first. Each model has its own page with its reports, recalls and device details.
- AIRFIT F20 63400Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AIRFIT F20 63401Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AIRFIT F20 63402Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AIRFIT F20 63403Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AIRFIT F20 63404Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AIRFIT F20 63445Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AIRFIT F20 63446Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AIRFIT F20 63447Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AIRFIT F20 63448Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AIRFIT F20 63449Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AIRFIT F20 63450Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AIRFIT F20 63456Ventilator, Non-Continuous (Respirator)1 recall0 reports
Other Resmed Pty Ltd products
- Astral3 models · 3,253 reports · 1 recall
- AIRFIT F30I10 models · 4 reports · 1 recall
- AIRFIT N 107 models · 0 reports · 1 recall
- AIRFIT N2013 models · 0 reports · 1 recall
- AirTouch F2016 models · 0 reports · 1 recall
- AirFit F305 models · 0 reports · 1 recall
- AirTouch N209 models · 0 reports · 1 recall
- AIRSENSE5 models · 44 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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