Centricity Universal Viewer Software Versions 5 — Class II medical device recall Z-1571-2026
Ongoing recall by GE Medical Systems, LLC, reported 2026-03-25, distributed nationwide. There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. Us
| Recall number | Z-1571-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Medical Systems, LLC, Waukesha, WI, United States |
| Recall initiated | 2026-01-30 |
| Classified | 2026-03-16 |
| Reported by FDA | 2026-03-25 |
| Distributed | Nationwide (US) |
| Quantity | 40 units |
| Reason classes | software |
| Model numbers | 2066908-136, 2066908-150, 2088026-003, 2088026-026, 2088026-043, 2088026-110, 2088026-115, 2088026-132, 2089629-003, K2042VJED |
Product
Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-026, 2088026-115, 2088026-043, K2042VJED, 2088026-132, 2088026-003, 2088026-110, 2089629-003, 2066908-136, 2066908-150
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1571-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.