Class II — Eizo Corporation
| Recalling firm | EIZO GmbH |
|---|---|
| Registered facility | EIZO GmbH (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | EIZO is recalling the RadiForce LCD Monitors could display abnormally while connecting to particular graphics boards with DisplayPort. |
| Product | RadiForce GX540, 5MP Monochrome LCD Monitor, Part Code No. 0FTD1826A5, 0FTD1826B5, 0FTD1826C5, UPC 690592034752. This product is intended to be used in displaying and viewing digital images including those of digital mammography for review and analysis by trained medical practitioners. |
| Quantity | 19 units |
| Distribution | Nationwide Distribution including OH, FL, IL, TX, OH, NY, AZ, and NJ. |
| Initiated | 2015-07-07 |
| Classified | 2015-07-16 |
| Terminated | 2016-11-30 |
| Recall number | Z-2087-2015 |
| 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-2087-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/71628/
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