Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Astral 100 ( Model No. 27001) & Astral 150 (Model No. 27003) ventilator. Recalled by ResMed Ltd. Due to The Astral device allows clinicians to disable all...
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 Ltd. directly.
Affected Products
Astral 100 ( Model No. 27001) & Astral 150 (Model No. 27003) ventilator.
Quantity: 1519 units
Why Was This Recalled?
The Astral device allows clinicians to disable all alarms including those that detect circuit disconnection. Inappropriate disabling of alarms in ventilator dependent patients can lead to hazards of insufficient ventilation and insufficient expiratory pressure which can result in major severity harm.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ResMed Ltd.
ResMed Ltd. has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report