KSIClass 2
Lectins And Protectins
FDA adverse event reports and recall history for lectins and protectins (product code KSI), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 701
- Deaths
- 0
- Injuries
- 0
- Malfunctions
- 701
Reports per year
116
70025
Source: FDA adverse event reports by year received, 2016–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor lectins and protectins automatically
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