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GE Healthcare, LLC recalls Centricity Universal Viewer and Viewer 6.0 - Product Usage: Is a device that displays medical images (including mammogra
Recalled September 29, 2021 · FDA recall Z-2503-2021 · GE Healthcare
Hazard
Image acquisition failures and synchronization failure with the Centricity Enterprise Archive · FDA Class II
Units
462 (279 US; 183 OUS)
Sold at
AK, AZ, CA, CO, DE, FL, GA, IA, IN, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NJ, NM, NV, NY, OH, OK, OR, PA, SD, TX, UT, WA, WI, WV and WY. Austria, Brazil, Canada, France, Germany, Ghana, India, Ireland, Israel, Italy, Kuwait, Netherlands, Panama, Poland, Russia, Saudi Arabia, Slovenia, South Africa, Spain, Switzerland, Turkey, United Kingdom and Uruguay.
Description
Image acquisition failures and synchronization failure with the Centricity Enterprise Archive
Product
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.
Manufacturer(s)
GE Healthcare, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →