QJIClass 2
Interoperable Automated Glycemic Controller
FDA adverse event reports and recall history for interoperable automated glycemic controller (product code QJI), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 3,009
- Deaths
- 3
- Injuries
- 899
- Malfunctions
- 2,104
Reports per year
120
121
422
2623
1524
325
2,95926
Source: FDA adverse event reports by year received, 2020–2026. 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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