Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BiPAP A30 Recalled by Philips Respironics, Inc. Due to Certain devices were built with motor assemblies that...
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 A30, Brazil: Continuous ventilator, non-life-supporting. Material Number: BR1111143
Quantity: 2 units
Why Was This Recalled?
Certain devices were built with motor assemblies that could contain non-conforming plastic material. This could result in 1. Exposure to off-gassing of Volatile Organic Compounds not normally present creating a potential biosafety or toxicological hazard and 2. Sudden failure of the device causing a Ventilator Inoperative condition with the potential for asphyxia if not immediately identified and addressed by the care provider.
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