2026 data FDA MAUDE openFDA FDA Class III

Stimulator, Electrical, Implanted, For Parkinsonian Symptoms

Adverse-event figures are drawn from the U.S. Food & Drug Administration (FDA) MAUDE database, refreshed March 2026, see our methodology.

OpenFDA device adverse-event casebook.

FDA MAUDE casebook

openFDA event book Stimulator LIGHT-BOOK · MAUDE

#522 of 1000 · 1,810 reports · 2003–2026

  • BOOK 1,810 reports
  • RANK #522 of 1000
  • DEATH 41 death-typed
  • INJ 1,588 injury-typed
  • MALF 179 malfunction
  • SPAN 2003–2026
  • PEAK 2023: 411
  • PHOTO Generator

Nearest event-volume peer: Generator, Lesion, Radiofrequency (2 report gap)

Stimulator, Electrical, Implanted, For Parkinsonian Symptoms sits #522 of 1000 among tracked device types with 1,810 MAUDE reports spanning 2003–2026. Rank counts report volume, not confirmed device fault. Event_type Death / Injury / Malfunction are one code per report — not the same population as patient-outcome rows ( methodology). Read with this device → · Lead manufacturer → · Similar-volume device →

Injury-coded reports run above the device-type norm

Stimulator carries 87.7% INJURY-coded reports, 57.4pp above the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.

  • DEATH 2.3% corpus 1.5% · above corpus mean (+0.8 pp)
  • INJ 87.7% corpus 30.3% · above corpus mean (+57.4 pp)
  • MALF 9.9% corpus 64.8% · below corpus mean (-54.9 pp)

Lead product-problem code Adverse Event Without Identified Device or Use Problem is 48% of coded problems · Lead manufacturer BOSTON SCIENTIFIC NEUROMODULATION accounts for 77% of manufacturer-tagged reports · Top event location is 76% of location-tagged rows .

Stimulator in the event-volume neighbourhood

FDA MAUDE report totals among this device type and nearest nationwide peers

reports

What this shows Stimulator, Electrical, Implanted, For Parkinsonian Symptoms carries 1,810 MAUDE reports, ranked #522 of 1000.

Source FDA MAUDE via openFDA, aggregated by PlainHospital As of August 2026

Event Types

Injury 1,588 (87.7%)
Malfunction 179 (9.9%)
Death 41 (2.3%)
Other 2 (0.1%)

Patient Outcomes

FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.

Required Intervention 1,297 (61.2%)
Hospitalization 258 (12.2%)
R 178 (8.4%)
136 (6.4%)
H 93 (4.4%)
Other 67 (3.2%)
Death 39 (1.8%)
O 29 (1.4%)
D 7 (0.3%)
S 6 (0.3%)
Life Threatening 4 (0.2%)
L 3 (0.1%)
Disability 2 (0.1%)

Top Product Problems

Adverse Event Without Identified Device or Use Problem 1,031
Unexpected Therapeutic Results 330
High impedance 147
Migration 135
Charging Problem 79
Battery Problem 61
Wireless Communication Problem 61
Inappropriate/Inadequate Shock/Stimulation 43
Use of Device Problem 36
Intermittent Energy Output 35
Premature Discharge of Battery 31
Fracture 29
Inappropriate or Unexpected Reset 21
Defective Device 15
Off-Label Use 15
Delayed Charge Time 13
Overheating of Device 13
Low impedance 12
Appropriate Device Problem Term/Code Not Available 11
Positioning Problem 10

Yearly Trend

03
2003: 1
12
2012: 1
17
2017: 3
18
2018: 66
19
2019: 74
20
2020: 146
21
2021: 205
22
2022: 214
23
2023: 411
24
2024: 399
25
2025: 194
26
2026: 96

Reports fell to 194 in 2025, down from an average of 405 in the two years before.

Related Entities for Stimulator, Electrical, Implanted, For Parkinsonian Symptoms

Event Locations

1,378 (76.1%)
I 418 (23.1%)
NO INFORMATION 8 (0.4%)
HOSPITAL 5 (0.3%)
UNKNOWN 1 (0.1%)

Compare BOSTON SCIENTIFIC NEUROMODULATION vs BOSTON SCIENTIFIC NEUROMODULATION CORPORATION →

Nationwide devices with a comparable volume-and-death footprint

Two openFDA-derived peer sets for Stimulator: nearest by total report volume and nearest by death-typed count, each floored at ≥100 reports so the neighborhoods stay in the advertised mass.

Disclaimer: MAUDE figures for Stimulator are informational only and are not clinical advice. Report codes do not prove device causation. Consult a qualified clinician before acting on this data.

Every figure on PlainHospital is rendered directly from federal source data, no number is typed in by an editor. Event-type mix on this page is computed from FDA MAUDE codes for Stimulator; corpus means use device types with ≥100 reports. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.