Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Philips OmniLab Advanced+ Intl (Flow Gen) Recalled by Philips Respironics, Inc. Due to Motor assemblies manufactured with nonconforming plastic that contributes...
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
Philips OmniLab Advanced+ Intl (Flow Gen), Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
Quantity: 34 units ***updated January 2024 *** additional 3 units
Why Was This Recalled?
Motor assemblies manufactured with nonconforming plastic that contributes to off-gassing of VOCs.
Where Was This Sold?
This product was distributed to 42 states: AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MA, MI, MN, MS, MO, MT, NV, NH, NJ, NY, NC, ND, OH, OK, OR, PA, TN, TX, VT, VA, WA, WV, WI, WY
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