Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Astral 100 Recalled by Resmed Corporation Due to Resmed Corporation is recalling Astral 100, 150 External...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Resmed Corporation directly.
Affected Products
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 possible that there may be scenarios where critically dependent patients may encounter this scenario, the likelihood of this leading to harm is negligible because critically dependent patients will have a form of backup ventilation as standard of care.
Quantity: 14,736
Why Was This Recalled?
Resmed Corporation is recalling Astral 100, 150 External Battery because of a start-up issue.
Where Was This Sold?
This product was distributed to 32 states: AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, KY, LA, MI, MN, MO, MT, NE, NH, NJ, NY, NC, OK, PA, RI, SC, TN, TX, UT, VA, WV, WY
About Resmed Corporation
Resmed Corporation has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report