ResMed Ltd. recalls
Every recall we track for ResMed Ltd. — 10 in all, from 2019–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from ResMed Ltd. peaked in 2023 (8); 10 since 2017.
All FDA recall records for ResMed Ltd. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 1 | 0 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 8 | 0 | 0 | 8 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 1 | 0 | 0 | 1 |
What to do if you have a recalled ResMed Ltd. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All ResMed Ltd. recalls
4 shown- Use cautionMedical device
ResMed Ltd. recalls Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory
ResMed recalls Astral 100/150 and 100/50 ventilators due to supercapacitor electrolyte leakage that may damage charger chips, causing ventilation interruptions. Affected units have specific serial numbers and model codes.
ResMedJun 25, 2026 - Use cautionMedical device
ResMed Ltd. recalls AirTouch F20 Full Face Mask and User Guide
ResMed recalls AirTouch F20 Full Face Masks with magnets that could interfere with medical implants. Affected units include specific model lots sold from 2020. Contact ResMed for details.
ResMedNov 20, 2023 - Use cautionMedical device
ResMed Ltd. recalls Astral 100 and Astral 150 ventilators
ResMed recalls Astral 100 and 150 ventilators made between 2013-2019 due to potential power failure causing ventilation to stop. Check serial numbers for affected units.
ResMedSep 13, 2023 - Use cautionMedical device
ResMed Ltd. recalls ResMed Stellar, Non-invasive/invasive ventilators, Model: 100, 150
ResMed recalls Stellar ventilators (Models 100/150) with serial numbers 20160123307-22171057208 due to potential alarm failure if stored without AC power for over 36 hours.
ResMedDec 12, 2019
ResMed Ltd. recall questions
How many recalls has ResMed Ltd. had?
10 recalls from ResMed Ltd. are on record with U.S. safety agencies, from 2019–2026.
What is the most recent ResMed Ltd. recall?
ResMed Ltd. recalls Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory, dated Jun 25, 2026. Every ResMed Ltd. recall is listed on this page, newest first.
What should I do if I have a recalled ResMed Ltd. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new ResMed Ltd. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.