GE Healthcare Centricity Universal Viewer Zero Footprint Client — Class II medical device recall Z-1475-2026
Ongoing recall by GE Healthcare, reported 2026-03-11, distributed nationwide. Under certain workflows, patient information shown in the viewer may not match the images displayed on Centric
| Recall number | Z-1475-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, Chicago, IL, United States |
| Recall initiated | 2026-01-16 |
| Classified | 2026-02-27 |
| Reported by FDA | 2026-03-11 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, BR, CA, CH, CN, DE, ES, FR, GB, ID, IE, IL, IN, IT, JP, KR, KW, LB, MY, NL, PH, PL, RU, SA, SE, SG, TW, VN, ZA |
| Quantity | 250 units |
| UPC / GTIN / UDI-DI | 00840682102988 |
| Model numbers | 2110344-039, 2110344-046, 2110344-047 |
Product
GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: 2110344-039, 2110344-046, 2110344-047; System, Image Processing, Radiological
Reason for recall
Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP) with versions ZFP v6.0: SP11.6, SP11.6.0.1 and SP11.6.1 on systems with Patient Timeline installed,
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-1475-2026. 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.