Implant, Anti-Gastroesophageal Reflux
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 Implant, Anti-Gastroesophageal Reflux LIGHT-BOOK · MAUDE
#469 of 1000 · 2,236 reports · 1992–2026
- BOOK 2,236 reports
- RANK #469 of 1000
- DEATH 2 death-typed
- INJ 2,112 injury-typed
- MALF 103 malfunction
- SPAN 1992–2026
- PEAK 2019: 280
- PHOTO Tray
Nearest event-volume peer: Tray, Surgical, Instrument (5 report gap)
Implant, Anti-Gastroesophageal Reflux sits #469 of 1000 among tracked device types with 2,236 MAUDE reports spanning 1992–2026. 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
Implant, Anti-Gastroesophageal Reflux carries 94.5% INJURY-coded reports, 64.2pp above the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.
- DEATH 0.1% corpus 1.5% · below corpus mean (-1.4 pp)
- INJ 94.5% corpus 30.3% · above corpus mean (+64.2 pp)
- MALF 4.6% corpus 64.8% · below corpus mean (-60.2 pp)
Lead product-problem code Adverse Event Without Identified Device or Use Problem is 36% of coded problems · Lead manufacturer UNK accounts for 100% of manufacturer-tagged reports · Top event location is 51% of location-tagged rows .
Implant, Anti-Gastroesophageal Reflux in the event-volume neighbourhood
FDA MAUDE report totals among this device type and nearest nationwide peers
- Implant (this)
Implant, Anti-Gastroesophageal Reflux
2,236 reports
- Tray
Tray, Surgical, Instrument
2,231 reports
- Stimulator
Stimulator, Electrical, Implanted, For Essential Tremor
2,224 reports
- Warmer
Warmer, Blood, Non-Electromagnetic Radiation
2,219 reports
- Forceps
Forceps
2,217 reports
- Endoscopic Gr…
Endoscopic Grasping/Cutting Instrument, Non-Powered
2,211 reports
What this shows Implant, Anti-Gastroesophageal Reflux carries 2,236 MAUDE reports, ranked #469 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 (165) held close to the prior two-year average of 207.
Related Entities for Implant, Anti-Gastroesophageal Reflux
Top Manufacturers
Event Locations
Nationwide devices with a comparable volume-and-death footprint
Two openFDA-derived peer sets for Implant, Anti-Gastroesophageal Reflux: 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 (2,236 here).
Similar death-typed counts
Nearest other device types by death-typed report count (2 here), distinct from the volume row.
Read our methodology - how this data is sourced, computed, and verified.
Disclaimer: MAUDE figures for Implant, Anti-Gastroesophageal Reflux 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 Implant, Anti-Gastroesophageal Reflux; 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.