QDKClass 2
Integrated Continuous Glucose Monitoring System For Non-Intensive Diabetes Management
FDA adverse event reports and recall history for integrated continuous glucose monitoring system for non-intensive diabetes management (product code QDK), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 620
- Deaths
- 1
- Injuries
- 18
- Malfunctions
- 601
Reports per year
218
2619
1820
11121
8122
7823
23824
6625
Source: FDA adverse event reports by year received, 2018–2025. 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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