Official recall record
Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and dat
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-01-30
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00840682103800
- Brand on record
- GE Medical Systems, LLC
What the authority reported
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-05-31.
Same barcode in other registries
The same EAN appears in 1 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.
- 2022-07-15 · US FDA — Medical Devices
(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX; (3
Other recalls from this brand
- 2026-06-05 · US FDA — Medical Devices
Optima XR200amx, Mobile Digital-Ready Radiographic System - 2026-06-05 · US FDA — Medical Devices
Optima XR240amx, Mobile Digital Radiographic System - 2026-06-05 · US FDA — Medical Devices
Optima XR220amx, Mobile Digital-Ready Radiographic System
All 62 official recall notices naming GE Medical Systems, LLC on this site →