Magstim 200² 3010-00Recalls & reported problems
The Magstim Company Limited · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05060229530424), received between Oct 17, 2025 and Oct 17, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Convulsion, Clonic1
- Convulsion, Tonic1
- Convulsion/Seizure1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 17, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
A MAGSTIM EMPLOYEE READ AN ARTICLE WHEREBY A 59-YEAR-OLD MALE STROKE SURVIVOR UNDERWENT SINGLE-PULSE TMS USING A BISTIM AND D70 COIL. APPROXIMATELY 5 MIN POST-STIMULATION, HE DEVELOPED A GENERALIZED TONIC-CLONIC SEIZURE. MULTIPLE SEIZURES FOLLOWED DURING TRANSPORT AND HOSPITAL ADMISSION. HE RECOVERED AFTER 2 DAYS. NO REPORTS OF THIS EVENT WERE MADE TO MAGSTIM DIRECTLY, THE INVESTIGATORS CONDUCTING THE TMS STUDY (THE AUTHORS OF THE PAPER) REPORTED THE EVENT TO THE METROHEALTH INSTITUTIONAL REVIEW BOARD (IRB). PAPER CITATION: YUK, J., HOGAN, S., WILSON, R. D., KNUTSON, J., & CUNNINGHAM, D. A. (2025). GENERALIZED TONIC-CLONIC SEIZURE FOLLOWING SINGLE-PULSE TRANSCRANIAL MAGNETIC STIMULATION TO THE IPSILESIONAL PRIMARY MOTOR CORTEX IN A PARTICIPANT WITH CHRONIC STROKE. CLINICAL NEUROPHYSIOLOGY, 178, 2110944. NO FURTHER INFORMATION WAS PROVIDED BY THE AUTHOR OF THE PAPER FOLLOWING 3 ATTEMPTS TO CONTACT THEM BY MAGSTIM.
Patient problems: Convulsion, Clonic; Convulsion, Tonic; Convulsion/Seizure
MAUDE report 23324568 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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