MFRClass f
Stimulator, Brain, Implanted, For Behavior Modification
FDA adverse event reports and recall history for stimulator, brain, implanted, for behavior modification (product code MFR), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 250
- Deaths
- 5
- Injuries
- 149
- Malfunctions
- 95
Reports per year
104
205
2212
1813
3014
7115
5116
2417
718
520
921
122
223
124
125
Source: FDA adverse event reports by year received, 2004–2025. 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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