ResMed Ltd.
10 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous recall (Z-2735-2026) | ResMed Ltd. | 2026-07-28 |
| AirFit N10 Nasal Masks and User Guide recall (Z-0536-2024) | ResMed Ltd. | 2023-12-21 |
| AirFit F20 Full Face Mask and User Guide recall (Z-0537-2024) | ResMed Ltd. | 2023-12-21 |
| AirTouch F20 Full Face Mask and User Guide recall (Z-0538-2024) | ResMed Ltd. | 2023-12-21 |
| AirFit N20 Nasal Mask and User Guide recall (Z-0539-2024) | ResMed Ltd. | 2023-12-21 |
| AirTouch N20 Nasal Mask and User Guide recall (Z-0540-2024) | ResMed Ltd. | 2023-12-21 |
| AirFit F30 Full Face Mask and User Guide recall (Z-0541-2024) | ResMed Ltd. | 2023-12-21 |
| AirFit F30i Full Face Mask and User Guide recall (Z-0542-2024) | ResMed Ltd. | 2023-12-21 |
| Astral 100 and Astral 150 ventilators recall (Z-0111-2024) | ResMed Ltd. | 2023-10-23 |
| Astral 100 ( Model No. 27001) & Astral 150 (Model No. 27003) ventilator. recall (Z-1750-2015) | ResMed Ltd. | 2015-06-10 |
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Every clearance here is in the API, with alerts when new ones post.