Device recall
Z-2294-2020: RadiForce RX360, model 0FTD2346 - Product Usage: is a color LCD monitor…
FDA device recall · Class II · Eizo Corporation
Key facts
| Recall number (Z-number) | Z-2294-2020 |
|---|---|
| Recall event | 85299 |
| 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. |
| Product code | PGY |
| Recalling firm | Eizo Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K182591 |
| FEI number | 3000237660 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database