QHJClass 3
Sensor, Glucose, Implanted, Non-Adjunctive Use
FDA adverse event reports and recall history for sensor, glucose, implanted, non-adjunctive use (product code QHJ), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 2,371
- Deaths
- 0
- Injuries
- 1,215
- Malfunctions
- 1,156
Reports per year
1820
921
17322
34123
91524
63525
28026
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
- TerminatedProcess control
Eversense CGM SENSOR (FG-4200-00-301)-Continuous Glucose Monitor
Eversense Sensors have prematurely stopped functioning due to inadequate hydration of the sensor s glucose-sensing surface
Monitor sensor, glucose, implanted, non-adjunctive use automatically
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