Dorsal Root Ganglion Stimulator For Pain Relief
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 Dorsal Root Ganglion Stimulator For Pain Re… MID-BOOK · MAUDE
#143 of 1000 · 19,735 reports · 2016–2026
- BOOK 19,735 reports
- RANK #143 of 1000
- DEATH 32 death-typed
- INJ 19,457 injury-typed
- MALF 243 malfunction
- SPAN 2016–2026
- PEAK 2019: 2,549
- PHOTO Suture
Nearest event-volume peer: Suture, Nonabsorbable, Synthetic, Polypropylene (49 report gap)
Dorsal Root Ganglion Stimulator For Pain Relief sits #143 of 1000 among tracked device types with 19,735 MAUDE reports spanning 2016–2026. 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
Dorsal Root Ganglion Stimulator For Pain Re… carries 98.6% INJURY-coded reports, 68.3pp above the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.
- DEATH 0.2% corpus 1.5% · below corpus mean (-1.3 pp)
- INJ 98.6% corpus 30.3% · above corpus mean (+68.3 pp)
- MALF 1.2% corpus 64.8% · below corpus mean (-63.6 pp)
Lead product-problem code Adverse Event Without Identified Device or Use Problem is 29% of coded problems · Lead manufacturer ABBOTT MEDICAL accounts for 66% of manufacturer-tagged reports · Top event location I is 51% of location-tagged rows .
Dorsal Root Ganglion Stimulator For Pain Re… in the event-volume neighbourhood
FDA MAUDE report totals among this device type and nearest nationwide peers
- Catheter
Catheter, Intravascular, Diagnostic
20,128 reports
- Suture
Suture, Nonabsorbable, Synthetic, Polyethylene
20,010 reports
- Leadless Pace…
Leadless Pacemaker
19,964 reports
- Dorsal Root G… (this)
Dorsal Root Ganglion Stimulator For Pain Relief
19,735 reports
- Suture
Suture, Nonabsorbable, Synthetic, Polypropylene
19,686 reports
- System
System, Image Processing, Radiological
19,647 reports
What this shows Dorsal Root Ganglion Stimulator For Pain Relief carries 19,735 MAUDE reports, ranked #143 of 1000.
Event Types
Patient Outcomes
FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.
Top Product Problems
Yearly Trend
Reports in 2025 (1,985) held close to the prior two-year average of 1,950.
Related Entities for Dorsal Root Ganglion Stimulator For Pain Relief
Top Manufacturers
Event Locations
Compare ABBOTT MEDICAL vs ST. JUDE MEDICAL - NEUROMODULATION →
Nationwide devices with a comparable volume-and-death footprint
Two openFDA-derived peer sets for Dorsal Root Ganglion Stimulator For Pain Re…: nearest by total report volume and nearest by death-typed count, each floored at ≥100 reports so the neighborhoods stay in the advertised mass.
Similar report volume
Nearest other device types by FDA MAUDE report count (19,735 here).
Similar death-typed counts
Nearest other device types by death-typed report count (32 here), distinct from the volume row.
Read our methodology - how this data is sourced, computed, and verified.
Disclaimer: MAUDE figures for Dorsal Root Ganglion Stimulator For Pain Re… 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 Dorsal Root Ganglion Stimulator For Pain Re…; 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.