FDA Device recall Z-2294-2020
RadiForce RX360, model 0FTD2346 - Product Usage: is a color LCD monitor indicated for use in displaying radiological images for review, ana…
- FDA Device
- Class II
- ongoing
- Published 2020-06-17
On 2020-06-17 the FDA classified a Class II recall of RadiForce RX360, model 0FTD2346 - Product Usage: is a color LCD monitor indicated for use in displaying radiological images for review, ana… by Eizo, citing under certain conditions, a marble pattern infrequently appears on the monitor.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2294-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-07-30 |
| Published | 2020-06-17 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Eizo |
| Distribution | US |
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
Under certain conditions, a marble pattern infrequently appears on the monitor.
Identifiers
| code_info | RadiForce RX360, 1.0001 or earlier, UDI 04995047053279, 04995047053293. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2294-2020%22
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