SFIClass 3
Sensor, Glucose, Invasive, Component Of Automated Insulin Delivery System
FDA adverse event reports and recall history for sensor, glucose, invasive, component of automated insulin delivery system (product code SFI), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 3,036
- Deaths
- 0
- Injuries
- 66
- Malfunctions
- 2,970
Reports per year
14225
2,89426
Source: FDA adverse event reports by year received, 2025–2026. 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.
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