Device recall
Z-1965-2020: Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is indicated for…
FDA device recall · Class II · The Magstim Company Limited
Key facts
| Recall number (Z-number) | Z-1965-2020 |
|---|---|
| Recall event | 85393 |
| Product | Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is indicated for the treatment of Major Depressive Disorder in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode. |
| Product code | OBP |
| Recalling firm | The Magstim Company Limited |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 20, 2024 |
| 510(k) numbers | K051864, K143531, K162935, K180907, K182853, K183376 |
| FEI number | 3002808356 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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