FDAJanuary 13, 2016device
Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily used as non-invasive homecare devices, for example, the largest population of patients on the Astral device is COPD patients primarily using the device at night with some daytime use for recovery breathing. While it is po...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Resmed Corporation is recalling Astral 100, 150 External Battery because of a start-up issue.
What to do
FDA enforcement status: Terminated
Brands named
resmed
UPCs
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Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAAirFit F20 Full Face Mask and User Guide2023-11-20
- FDAAirFit N10 Nasal Masks and User Guide2023-11-20
- FDAAirFit N20 Nasal Mask and User Guide2023-11-20
- FDAAirTouch N20 Nasal Mask and User Guide2023-11-20
- FDAAirFit F30 Full Face Mask and User Guide2023-11-20
- FDAAirFit F30i Full Face Mask and User Guide2023-11-20
- FDAAirTouch F20 Full Face Mask and User Guide2023-11-20
- FDAAstral 100 and Astral 150 ventilators2023-09-13
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