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/AEMS corpus and the live FDA recall database.
- Total reports
- 1,985
- Deaths
- 2
- Injuries
- 620
- Malfunctions
- 1,360
Reports per year
120
121
422
2623
1524
325
1,93526
Source: FDA adverse event reports by year received, 2020–2026. 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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