Stimulator, electrical, implanted, for essential tremor
FDA product code PJS · Class 3 · 14 devices · 1,282 reports · 30 deaths reported · 5 devices named in recalls
- Vercise Genus™ DB-1216Boston Scientific Neuromodulation Corporation · Stimulator, electrical, implanted, for essential tremor2 recalls23 deaths584 reports
- Liberta RC™ 62400Advanced Neuromodulation Systems, Inc. · Stimulator, electrical, implanted, for essential tremor2 recalls1 death103 reports
- SureTek™ DB-4600-CBoston Scientific Neuromodulation Corporation · Stimulator, electrical, implanted, for essential tremor1 recall138 reports
- Activa® SC 37603Medtronic, Inc. · Stimulator, electrical, implanted, for essential tremor1 recall111 reports
- Activa® SC 37602Medtronic, Inc. · Stimulator, electrical, implanted, for essential tremor1 recall85 reports
- SenSight™ B3301542Medtronic, Inc. · Stimulator, electrical, implanted, for essential tremor3 deaths77 reports
- N/A 3708660Medtronic, Inc. · Stimulator, electrical, implanted, for essential tremor43 reports
- SenSight™ B3301542MMedtronic, Inc. · Stimulator, electrical, implanted, for essential tremor3 deaths43 reports
- NA DB-3128-55BBoston Scientific Neuromodulation Corporation · Stimulator, electrical, implanted, for essential tremor38 reports
- Vercise™ DB-9218-15Boston Scientific Neuromodulation Corporation · Stimulator, electrical, implanted, for essential tremor25 reports
- NA 16000Thoratec Corporation · Stimulator, electrical, implanted, for essential tremor15 reports
- Vercise Genus™ DB-1408Boston Scientific Neuromodulation Corporation · Stimulator, electrical, implanted, for essential tremor12 reports
- NA SC-4254Boston Scientific Neuromodulation Corporation · Stimulator, electrical, implanted, for essential tremor7 reports
- SenSight™ B3400095MMedtronic, Inc. · Stimulator, electrical, implanted, for essential tremor1 report