Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
ResMed Stellar Recalled by ResMed Ltd. Due to Combination of software and a component failure may...
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
ResMed Stellar, Non-invasive/invasive ventilators, Model: 100, 150
Quantity: 69
Why Was This Recalled?
Combination of software and a component failure may cause audible alarms not to operate properly, the alarm buzzer not work, for ventilators that have a failed electronic component and, that are stored without AC power connected for more than 36 hours leading to full depletion of the battery and, that powers on automatically when connected to AC power without pressing the power switch.
Where Was This Sold?
This product was distributed to 9 states: CT, FL, GA, IL, MA, MT, PA, TN, VA
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