GE Healthcare Centricity Universal Viewer Zero Footprint Client — Class II medical device recall Z-3160-2024
Ongoing recall by GE Healthcare, reported 2024-09-25. Footprint Client (ZFP) versions v6.0 SP9.x and SP10.x where the latest addended report is not shown by default
| Recall number | Z-3160-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, Chicago, IL, United States |
| Recall initiated | 2024-07-23 |
| Classified | 2024-09-17 |
| Reported by FDA | 2024-09-25 |
| Quantity | 803 units |
| UPC / GTIN / UDI-DI | 00840682102988 |
Product
GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: a) 2110344-008; b) 2110344-009; c) 2110344-010; d) 2110344-011; e) 2110344-013; f) 2110344-019; g) 2110344-025; h) 2110344-029; i) 2110344-030; j) 2110344-032 ; Radiological image processing system
Reason for recall
Footprint Client (ZFP) versions v6.0 SP9.x and SP10.x where the latest addended report is not shown by default to the user. The issue occurs when the addendum is created on the same day as the original report but at a different time, and only when launched on the following browsers. " Internet Explorer 10 (IE10) " Internet Explorer 11 (IE11) " Firefox.
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-3160-2024. 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.