Class II — Eizo Corporation
| Recalling firm | EIZO GmbH |
|---|---|
| Registered facility | EIZO GmbH (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Under certain conditions, a marble pattern infrequently appears on the monitor. |
| 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. |
| Quantity | 1,466 monitors dist. to the U.S. |
| Distribution | Worldwide distribution - US Nationwide distribution including in the states of Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Illinois, Indiana, Kansas, Louisiana, Maine, Massachusetts, Michigan, Missouri, Montana, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, South Dakota, Tennessee, Texas, Virg… |
| Initiated | 2019-07-30 |
| Classified | 2020-06-08 |
| Recall number | Z-2294-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Eizo Corporation (Z-2294-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/85299/
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