Centricity Universal Viewer with Cross Enterprise Display This… — Class II medical device recall Z-0195-2019
Terminated recall by GE Healthcare, LLC, reported 2018-10-24, distributed in NY. Remote comparison studies displayed may be associated with the wrong patient, without a caution icon present.
| Recall number | Z-0195-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, LLC, Waukesha, WI, United States |
| Recall initiated | 2018-08-30 |
| Classified | 2018-10-18 |
| Reported by FDA | 2018-10-24 |
| Terminated | 2022-08-31 |
| Distributed | NY |
| Quantity | 1 |
Product
Centricity Universal Viewer with Cross Enterprise Display This impacts product versions 6.0 SP1 and higher.
Reason for recall
Remote comparison studies displayed may be associated with the wrong patient, without a caution icon present.
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-0195-2019. 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.