Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GE Datex-Ohmeda Avance CS2 Anesthesia System - Product Usage: intended Recalled by GE Healthcare, LLC Due to Flow sensors could have damaged tubes in the...
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 GE Healthcare, LLC directly.
Affected Products
GE Datex-Ohmeda Avance CS2 Anesthesia System - Product Usage: intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (neonatal, pediatric, adult). The device is intended for volume or pressure control ventilation.
Quantity: 88 devices
Why Was This Recalled?
Flow sensors could have damaged tubes in the form of small punctures or cuts.
Where Was This Sold?
This product was distributed to 36 states: AL, AZ, AR, CA, CO, FL, GA, ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MS, MO, MT, NE, NV, NJ, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI
About GE Healthcare, LLC
GE Healthcare, LLC has 474 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report