Tosoh Corporation
FDA adverse event reports naming Tosoh Corporation as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: TOSOH CORPORATION.
- Total reports
- 4,787
- Deaths
- 0
- Injuries
- 14
- Malfunctions
- 4,772
Reports per year
194
104
205
315
716
17117
3,78218
46919
23520
11621
Source: FDA adverse event reports by year received, 1994–2021. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Fluorometer, For Clinical UseKHO2,743
- Assay, Glycosylated HemoglobinLCP2,028
- Device, Angioplasty, Laser, CoronaryLPC5
- Radioimmunoassay, Testosterones And DihydrotestosteroneCDZ3
- Radioimmunoassay, EstradiolCHP1
- Counter, Cell, Automated (Particle Counter)GKL1
- Visual, Pregnancy Hcg, Prescription UseJHI1
- Analyzer, Chemistry (Sequential Multiple, Continuous Flow) Clinical UseJJC1
- Analyzer, Chemistry (Photometric, Discrete), For Clinical UseJJE1
- Acid, Pyruvic, Enzymatic (U.V.)JLT1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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