Device recall
Z-2429-2020: Oscar 2, Model 250 System
FDA device recall · Class II · Suntech Medical, Inc.
Key facts
| Recall number (Z-number) | Z-2429-2020 |
|---|---|
| Recall event | 85515 |
| Product | Oscar 2, Model 250 System |
| Product code | DXN |
| Recalling firm | Suntech Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 13, 2023 |
| 510(k) numbers | K151520 |
| FEI number | 1036863 |
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