Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Discovery IGS 740 Interventional Fluoroscopic X-ray Systems Recalled by GE Medical Systems, SCS Due to The Discovery IGS and Innova IGS systems may...
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 Medical Systems, SCS directly.
Affected Products
Discovery IGS 740 Interventional Fluoroscopic X-ray Systems
Quantity: 102 devices total
Why Was This Recalled?
The Discovery IGS and Innova IGS systems may experience X-ray abort errors which could result in the loss of imaging mode before or during fluoroscopic use.
Where Was This Sold?
This product was distributed to 16 states: AR, CA, FL, GA, IL, IA, NH, NJ, NM, NY, NC, PA, SC, TN, WV, WI
About GE Medical Systems, SCS
GE Medical Systems, SCS has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report