Device recall
Z-0156-2020: V-Twin, Catalog # 6002-800, UDI # 03661540600180 Product Usage: automated…
FDA device recall · Class II · Vital Scientific N.V.
Key facts
| Recall number (Z-number) | Z-0156-2020 |
|---|---|
| Recall event | 83582 |
| Product | V-Twin, Catalog # 6002-800, UDI # 03661540600180 Product Usage: automated chemistry analyzer intended for clinical use |
| Product code | JJF |
| Recalling firm | Vital Scientific N.V. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 19, 2024 |
| 510(k) numbers | K973628 |
| FEI number | 2708 |
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