GE Centricity Universal Viewer Zero Footprint Client — Class II medical device recall Z-0329-2022
Terminated recall by GE Healthcare, LLC, reported 2021-12-08, distributed nationwide. There is a potential to display incomplete patient imaging study.
| Recall number | Z-0329-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, LLC, Waukesha, WI, United States |
| Recall initiated | 2021-10-15 |
| Classified | 2021-12-02 |
| Reported by FDA | 2021-12-08 |
| Terminated | 2026-08-17 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AU, AW, BE, BO, BR, CA, CH, CL, CN, CO, DE, DO, EC, ES, FR, GB, ID, IE, IL, IN, IT, JP, KR, KW, LB, MX, MY, PA, QA, RU, SA, TR, TT, TW, VN, ZA |
| Quantity | 638 devices |
| UPC / GTIN / UDI-DI | 00840682102988 |
Product
GE Centricity Universal Viewer Zero Footprint Client
Reason for recall
There is a potential to display incomplete patient imaging study.
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-0329-2022. 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.