Device recall
Z-2442-2020: Leksell Vantage Stereotactic System, UDI/GTIN 7340048304887
FDA device recall · Class II · Elekta Instrument AB
Key facts
| Recall number (Z-number) | Z-2442-2020 |
|---|---|
| Recall event | 85836 |
| Product | Leksell Vantage Stereotactic System, UDI/GTIN 7340048304887 |
| Product code | HAW |
| Recalling firm | Elekta Instrument AB |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 27, 2024 |
| 510(k) numbers | K171123 |
| FEI number | 3002806883 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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