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 corpus and the live FDA recall database.
- Total reports
- 2,224
- Deaths
- 5
- Injuries
- 734
- Malfunctions
- 1,485
Reports per year
116
219
1520
20221
29422
54323
49424
42625
24726
Source: FDA adverse event reports by year received, 2016–2026. 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.
Monitor stimulator, electrical, implanted, for essential tremor automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.