AirTouch F20Recalls & reported problems across all models
Resmed Pty Ltd · 16 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one AirTouch 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 16 models of AirTouch 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
AirTouch 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, 2023Open, 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-0538-2024 · Root cause: Device Design · names 16 of these models · Recall details · FDA record ↗
AirTouch F20 models
16 models, most reported first. Each model has its own page with its reports, recalls and device details.
- AirTouch F20 63000Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63001Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63002Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63003Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63004Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63005Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63006Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63007Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63008Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63009Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63013Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63014Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63015Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63016Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63017Ventilator, Non-Continuous (Respirator)1 recall0 reports
- AirTouch F20 63018Ventilator, 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
- AirFit F305 models · 0 reports · 1 recall
- AirTouch N209 models · 0 reports · 1 recall
- AIRFIT F2012 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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