The Magstim Company Limited: Medical Device Recalls in 2020
Updated on March 25, 2026.
According to to data from the FDA, there were 3 medical device recalls made by The Magstim Company Limited in 2020. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- Neurosign V4 Intraoperative Nerve monitor family of devices.
- 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.
- Rapid2 PSU Stim Interconnecting Cable - Product Usage: 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.