QIIClass 2
Integrated Continuous Glucose Monitoring System For Professional Directed Retrospective Or Real-Time Use
FDA adverse event reports and recall history for integrated continuous glucose monitoring system for professional directed retrospective or real-time use (product code QII), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 237
- Deaths
- 1
- Injuries
- 2
- Malfunctions
- 234
Reports per year
220
9321
5922
6223
1824
325
Source: FDA adverse event reports by year received, 2020–2025. 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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