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 corpus and the live FDA recall database.
- Total reports
- 403
- Deaths
- 2
- Injuries
- 187
- Malfunctions
- 214
Reports per year
818
3219
1820
3621
4422
6223
7324
8325
4726
Source: FDA adverse event reports by year received, 2018–2026. 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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