The Magstim Company Limited recalls
Every recall we track for The Magstim Company Limited — 6 in all, from 2017–2020 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from The Magstim Company Limited peaked in 2020 (4); 6 since 2017.
All FDA recall records for The Magstim Company Limited since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 1 | 0 | 1 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 2 | 1 | 1 | 4 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled The Magstim Company Limited product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All The Magstim Company Limited recalls
5 shown- Use cautionMedical device
The Magstim Company Limited recalls Neurosign 100, Product Number 9883-01. Intraoperative Nerve Monitor - Product Usage: indicated for use in stimulating
Magstim recalls Neurosign 100 nerve monitors with incorrect voltage settings for US/Canada use. These may cause electrical issues if connected to 120V power. Affected units have specific serial numbers.
MagstimDec 8, 2020 - Lower riskMedical device
The Magstim Company Limited recalls Neurosign V4 Intraoperative Nerve monitor family of devices.
Magstim recalls Neurosign V4 nerve monitors with serial numbers 001-049 due to potential cable damage from improper handling. Affected units may require repair or replacement.
MagstimJun 23, 2020 - Use cautionMedical device
The Magstim Company Limited recalls Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is indicated for the treatment of Major Depressive
Magstim recalls Horizon PSU Stim Interconnecting Cable due to potential high voltage cable failure. This could pose a risk of serious injury during use for major depressive disorder treatment.
MagstimMar 23, 2020 - Lower riskMedical device
The Magstim Company Limited recalls HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)
Magstim recalls HORIZON Ez Arm devices with specific serial numbers due to potential stray stainless-steel cable protrusion from heat shrink sleeving.
MagstimOct 25, 2018 - Lower riskMedical device
The Magstim Company Limited recalls Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air
Magstim recalls 4800-0:0T Rapid Therapy System units due to missing user manuals. This could affect safe use of the device for treating depression.
MagstimSep 28, 2017
The Magstim Company Limited recall questions
How many recalls has The Magstim Company Limited had?
6 recalls from The Magstim Company Limited are on record with U.S. safety agencies, from 2017–2020.
What is the most recent The Magstim Company Limited recall?
The Magstim Company Limited recalls Neurosign 100, Product Number 9883-01. Intraoperative Nerve Monitor - Product Usage: indicated for use in stimulating, dated Dec 8, 2020. Every The Magstim Company Limited recall is listed on this page, newest first.
What should I do if I have a recalled The Magstim Company Limited product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new The Magstim Company Limited recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.