Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GE Healthcare Avance CS2 Recalled by GE Healthcare, LLC Due to The base of the anesthesia system can have...
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 Healthcare Avance CS2, Avance CS2 Pro Anesthesia Systems, Part #1009-9050-000; and Aisys CS2 Anesthesia Systems, Part # 1011-9050-000.
Quantity: 667 devices
Why Was This Recalled?
The base of the anesthesia system can have a crack and could potentially fracture resulting in a tip or overbalance of the anesthesia system. This can result in potential injury if it falls on a person.
Where Was This Sold?
This product was distributed to 28 states: AZ, CA, CO, CT, FL, ID, IL, IN, IA, KY, LA, ME, MD, MA, MI, MO, MT, NE, NV, NY, NC, OH, PA, SC, TN, TX, VA, WV
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