Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
(1) GE Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to Inaccurate Distance and Area measurements with use of...
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
(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX; (3) GE Universal Viewer 8.0, Model 5865740-00x.
Quantity: 1,690 devices
Why Was This Recalled?
Inaccurate Distance and Area measurements with use of Global Stack viewport.
Where Was This Sold?
This product was distributed to 40 states: AZ, AR, CA, CO, DE, FL, GA, ID, IL, IN, IA, KS, LA, ME, MD, MA, MI, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, RI, SC, SD, TN, TX, VT, WA, WV, 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