Neuro - Villalba
FDA adverse event reports naming Neuro - Villalba as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: NEURO - VILLALBA.
- Total reports
- 2,658
- Deaths
- 15
- Injuries
- 1,241
- Malfunctions
- 1,402
Reports per year
6111
25012
33613
22914
71015
83516
3417
2318
2219
3320
6521
2722
1623
1124
425
Source: FDA adverse event reports by year received, 2011–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW1,103
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY949
- Stimulator, Electrical, Implantable, For IncontinenceEZW512
- Stimulator, Spinal-Cord, Implanted (Pain Relief)GZB49
- Implanted Subcortical Electrical Stimulator (Motor Disorders)MRU34
- Stimulator, Brain, Implanted, For Behavior ModificationMFR4
- Unit, Electrosurgical, Endoscopic (With Or Without Accessories)KNS3
- Stimulator, Electrical, Implanted, For Essential TremorPJS2
- Pump, Infusion, Implanted, ProgrammableLKK1
- Orthopedic Manual Surgical InstrumentLXH1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Neuro - Villalba 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.