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GE Healthcare, LLC recalls Centricity Universal Viewer with Cross Enterprise Display This impacts product versions 6.0 SP1 and higher.
Recalled October 24, 2018 · FDA recall Z-0195-2019 · GE Healthcare
Hazard
Remote comparison studies displayed may be associated with the wrong patient, without a caution icon present. · FDA Class II
Units
1
Sold at
NY
Description
Remote comparison studies displayed may be associated with the wrong patient, without a caution icon present.
Product
Centricity Universal Viewer with Cross Enterprise Display This impacts product versions 6.0 SP1 and higher.
Manufacturer(s)
GE Healthcare, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →