QCDClass 3
Continuous Glucose Monitor, Implanted, Adjunctive Use
FDA adverse event reports and recall history for continuous glucose monitor, implanted, adjunctive use (product code QCD), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 1,514
- Deaths
- 0
- Injuries
- 948
- Malfunctions
- 566
Reports per year
318
27019
57620
15721
2922
11523
36424
Source: FDA adverse event reports by year received, 2018–2024. 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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