MBXClass 3
Stimulator, Thalamic, Epilepsy, Implanted
FDA adverse event reports and recall history for stimulator, thalamic, epilepsy, implanted (product code MBX), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 397
- Deaths
- 2
- Injuries
- 184
- Malfunctions
- 211
Reports per year
818
3219
1820
3621
4422
6223
7324
8325
4126
Source: FDA adverse event reports by year received, 2018–2026. 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.
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