RadiForce RX360 — Class II medical device recall Z-2294-2020
Ongoing recall by Eizo Corporation, reported 2020-06-17, distributed nationwide. Under certain conditions, a marble pattern infrequently appears on the monitor.
| Recall number | Z-2294-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Eizo Corporation, Hakusan, N/A, Japan |
| Recall initiated | 2019-07-30 |
| Classified | 2020-06-08 |
| Reported by FDA | 2020-06-17 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BE, BR, CA, CH, CN, CZ, DE, EG, ES, FR, GB, GR, HK, IL, IN, IT, JP, KR, LB, MX, NL, PK, PL, RU, SA, SE, SG, TH, TR, TW, ZA |
| Quantity | 1,466 monitors |
| UPC / GTIN / UDI-DI | 04995047053279, 04995047053293 |
| Model numbers | 0FTD2346 |
Product
RadiForce RX360, model 0FTD2346 - Product Usage: is a color LCD monitor indicated for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners. The display is not intended for mammography.
Reason for recall
Under certain conditions, a marble pattern infrequently appears on the monitor.
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-2294-2020. 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.