Device recall
Z-1427-2017: Juno DRF; Model: 709020 Product Usage: General, multi-function x-ray systems…
FDA device recall · Class II · Villa Sistemi Medicali S.P.A.
Key facts
| Recall number (Z-number) | Z-1427-2017 |
|---|---|
| Recall event | 76367 |
| Product | Juno DRF; Model: 709020 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures |
| Product code | KXJ |
| Recalling firm | Villa Sistemi Medicali S.P.A. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 9, 2021 |
| 510(k) numbers | K050190 |
| FEI number | 3002808461 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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