PJSClass 3
Stimulator, Electrical, Implanted, For Essential Tremor
FDA adverse event reports and recall history for stimulator, electrical, implanted, for essential tremor (product code PJS), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 2,181
- Deaths
- 5
- Injuries
- 711
- Malfunctions
- 1,465
Reports per year
116
219
1520
20221
29422
54323
49324
42625
20526
Source: FDA adverse event reports by year received, 2016–2026. 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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