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 corpus and the live FDA recall database.
- Total reports
- 3,653
- Deaths
- 0
- Injuries
- 72
- Malfunctions
- 3,581
Reports per year
14225
3,51126
Source: FDA adverse event reports by year received, 2025–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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