GE Centricity Universal Viewer Zero Footprint — Class II medical device recall Z-1333-2022
Ongoing recall by GE Healthcare, LLC, reported 2022-07-13. Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (Z
| Recall number | Z-1333-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, LLC, Waukesha, WI, United States |
| Recall initiated | 2022-06-08 |
| Classified | 2022-07-05 |
| Reported by FDA | 2022-07-13 |
| Quantity | 1,934 units |
| UPC / GTIN / UDI-DI | 00840682102988 |
Product
GE Centricity Universal Viewer Zero Footprint. To view, communicate, process, and display Medical images and data within a computer network or on a workstation.
Reason for recall
Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP)
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-1333-2022. 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.