inforMED
InjuryOBP

NEURONETICS, INC.

Received Jul 1, 2026 · Event occurred Jun 16, 2026

Report 3004824012-2026-00016 · MDR key 25683005

Device

Generic name

Tms

Manufacturer

Neuronetics, Inc.

Model number

V.3.8

Catalog number

81-05315-000

Product problems

  • Adverse Event Without Identified Device or Use Problem

Patient

Not reported

  • Convulsion/Seizure

Narrative

Additional Manufacturer Narrative

PATIENT EXPERIENCED A SEIZURE WHILE RECEIVING TMS THERAPY 3 MINUTES 40 SECONDS INTO HIS INITIAL TREATMENT. PROVIDER FEELS THE CAUSE IS MULTI-FACTORIAL: DEHYDRATION, WELLBUTRIN DOSING, TMS THERAPY, AND POSSIBLE ELECTROLYTE IMBALANCE AND LOW GLUCOSE.

Description of Event or Problem

PATIENT EXPERIENCED A SEIZURE WHILE RECEIVING THEIR FIRST DAILY TMS TREATMENT.