NEXSTIM PLC
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
Devices registered here (3)
- Stimulator, Electrical, Evoked ResponseProduct code GWF (opens in a new tab) · Class II · Neurology · 21 CFR 882.1870
- Neurological Stereotaxic InstrumentProduct code HAW (opens in a new tab) · Class II · Neurology · 21 CFR 882.4560
- Electromyograph, DiagnosticProduct code IKN (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.1375
Recalls & enforcement
- Class IIOngoing2017-03-14Software defect: the NBS software may accidentally generate duplicate copies of one or several files.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “NEXSTIM PLC (FEI 3007147067) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007147067-nexstim-plc/
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