Centricity Universal Viewer Workflow Manager — Class II medical device recall Z-0142-2024
Ongoing recall by GE Healthcare, reported 2023-11-01, distributed nationwide. When using Universal Viewer or Centricity Universal Viewer with Workflow Manager (WFM), if a third-party repor
| Recall number | Z-0142-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, Chicago, IL, United States |
| Recall initiated | 2023-09-08 |
| Classified | 2023-10-23 |
| Reported by FDA | 2023-11-01 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, CA, DE, FR, HK, IL, IT, PH, SG, TH, TR, VN |
| Quantity | 85 units |
| UPC / GTIN / UDI-DI | 00840682145794 |
Product
Centricity Universal Viewer Workflow Manager, Image processing radiological system
Reason for recall
When using Universal Viewer or Centricity Universal Viewer with Workflow Manager (WFM), if a third-party reporting application is used to launch exams, it could display information on a different patient than WFM and the Viewer.
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-0142-2024. 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.