Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
BiPAP V30 Auto Ventilator Recalled by Philips Respironics, Inc. Due to Potential for devices to experience interruption/loss of therapy...
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 Philips Respironics, Inc. directly.
Affected Products
BiPAP V30 Auto Ventilator, Part Number 1111178
Quantity: 5,958 US; None OUS
Why Was This Recalled?
Potential for devices to experience interruption/loss of therapy during a Ventilator Inoperative alarm. This may lead to hypoventilation, mild to severe hypoxemia, hypercarbia, respiratory failure/insufficiency, or potentially death in the most vulnerable patients.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Respironics, Inc.
Philips Respironics, Inc. has 85 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report