Device recall
Z-0836-2019: HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)
FDA device recall · Class II · The Magstim Company Limited
Key facts
| Recall number (Z-number) | Z-0836-2019 |
|---|---|
| Recall event | 81489 |
| Product | HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.) |
| Product code | OBP |
| Recalling firm | The Magstim Company Limited |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K180907 |
| 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