Device recall
Z-1352-2018: Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power…
FDA device recall · Class II · The Magstim Company Limited
Key facts
| Recall number (Z-number) | Z-1352-2018 |
|---|---|
| Recall event | 79577 |
| Product | Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air Film Coil and Main Filters Product Usage For the treatment of major depressive disorders in adult patients who have failed to achieve satisfactory improvement from prior… |
| Product code | OBP |
| Recalling firm | The Magstim Company Limited |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 21, 2022 |
| 510(k) numbers | K143531, K162935 |
| 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