Eizo Corporation Eizo Kabu Hakusan Japan 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. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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.
Brand
Eizo Corporation Eizo Kabu Hakusan Japan
Lot Codes / Batch Numbers
RadiForce RX360, 1.0001 or earlier, UDI 04995047053279, 04995047053293.
Products Sold
RadiForce RX360, 1.0001 or earlier, UDI 04995047053279, 04995047053293.
Eizo Corporation Eizo Kabu Hakusan Japan is recalling RadiForce RX360, model 0FTD2346 - Product Usage: is a color LCD monitor indicated for use in display due to Under certain conditions, a marble pattern infrequently appears on the monitor.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Under certain conditions, a marble pattern infrequently appears on the monitor.
Recommended Action
Per FDA guidance
EIZO Japan announced the recall on their website on 7/30/2019. EIZO U.S. began contacting their consignees via email and phone (one as early as 8/7/2019, some on 10/18/2019, but the majority on 11/26/2019) and began updating consignee monitors with the firmware. The notification requested the consignee contact EIZO U.S. for assistance with the firmware update.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026