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/AEMS 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 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.
Monitor continuous glucose monitor, implanted, adjunctive use automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.