Nihon Kohden Corporation
FDA adverse event reports naming Nihon Kohden Corporation as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: NIHON KOHDEN CORPORATION.
- Total reports
- 6,870
- Deaths
- 69
- Injuries
- 47
- Malfunctions
- 6,747
Reports per year
108
16914
21415
27216
39517
49918
74219
80620
1,63321
48622
35223
28624
63725
37826
Source: FDA adverse event reports by year received, 2008–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)MHX5,197
- Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)DRT515
- Analyzer, Gas, Carbon-Dioxide, Gaseous-PhaseCCK513
- Transmitters And Receivers, Physiological Signal, RadiofrequencyDRG470
- Stimulator, Electrical, Evoked ResponseGWF100
- Non-Normalizing Quantitative Electroencephalograph SoftwareOLT32
- Full-Montage Standard ElectroencephalographGWQ15
- System, Measurement, Blood-Pressure, Non-InvasiveDXN9
- ElectrocardiographDPS5
- Electromyograph, DiagnosticIKN5
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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