Device recall
Z-0547-2020: V-Twin, REF 6002-800 or 6002-850, SN 18-3304, IVD, (01)03661540600180
FDA device recall · Class II · Vital Scientific N.V.
Key facts
| Recall number (Z-number) | Z-0547-2020 |
|---|---|
| Recall event | 83910 |
| Product | V-Twin, REF 6002-800 or 6002-850, SN 18-3304, IVD, (01)03661540600180 |
| Product code | JJF |
| Recalling firm | Vital Scientific N.V. |
| Recall class | Class II |
| Status | Open, Classified |
| 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