Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Centricity Universal Viewer and Viewer 6.0 - Product Usage: Is Recalled by GE Healthcare, LLC Due to Image acquisition failures and synchronization failure with 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
Centricity Universal Viewer and Viewer 6.0 - Product Usage: Is a device that displays medical images (including mammograms) and data from various imaging sources. Includes the following Model Numbers: 1. Model Number: 2090255-001; 2. Model Number: 2088026-723; 3. Model Number: 2102676-001; 4. Model Number: 2104867-044.
Quantity: 462 (279 US; 183 OUS)
Why Was This Recalled?
Image acquisition failures and synchronization failure with the Centricity Enterprise Archive
Where Was This Sold?
This product was distributed to 34 states: AK, AZ, CA, CO, DE, FL, GA, IN, IA, LA, MD, MA, MI, MN, MS, MO, MT, NV, NJ, NM, NY, NC, ND, OH, OK, OR, PA, SD, TX, UT, WA, WV, WI, WY
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