Centricity Enterprise Web — Class II medical device recall Z-1230-2022
Ongoing recall by GE Healthcare, LLC, reported 2022-06-15, distributed nationwide. Potential for Distance and Area measurements to display inaccurate measurement values when performed on magnif
| Recall number | Z-1230-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, LLC, Waukesha, WI, United States |
| Recall initiated | 2022-04-28 |
| Classified | 2022-06-03 |
| Reported by FDA | 2022-06-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BE, BM, BO, BR, BS, CA, CH, CL, CN, CO, CR, DE, DK, DO, EC, EG, ES, FI, FR, GB, HK, HU, ID, IE, IL, IN, IT, JP, KR, KW, LB, MT, MX, MY, NG, NL, NO, PA, PE, PK, PL, PT, QA, RU, SA, SE, SG, TH, TR, TT, TW, UY, VE, VN, ZA |
| Quantity | 536 units |
Product
Centricity Enterprise Web
Reason for recall
Potential for Distance and Area measurements to display inaccurate measurement values when performed on magnified images, and specific to ZFP, Distance and Area measurements can display inaccurate measurement values when performed on lossy images that are scaled down from their original resolution.
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-1230-2022. 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.