FDAAugust 12, 2021device
Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
A software anomaly exists in the Centricity Universal Viewer study management feature in which study changes are not propagated to either the Centricity Enterprise Archive (EA) or another Vendor Neutral Archive (VNA).
What to do
FDA enforcement status: Terminated
Brands named
ge healthcare
UPCs
00840682145794
Recall history
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- FDAGE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL (64.7%), Rx Only, Distributed by: GE Healthcare Inc., Marlborough, MA 01752 USA, NDC 0407-1414-91.2026-03-24
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