RadiForce GX560 monochrome LCD monitor — Class II medical device recall Z-2293-2020
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-2293-2020 |
|---|---|
| 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 | 96 monitors |
| Model numbers | 0FTD2347, 0FTD2379 |
Product
RadiForce GX560 monochrome LCD monitor, models 0FTD2347 and 0FTD2379 - Product Usage: is indicated for use in displaying radiological images (including full-field digital mammography and digital breast tomosynthesis) for review, analysis, and diagnosis by trained medical practitioners.
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-2293-2020. 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.