Anesthesia Conduction Kit
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 Class II (moderate risk, special controls required), regulated under 21 CFR §868.5140 (Anesthesiology panel).
FDA MAUDE casebook
openFDA event book Anesthesia Conduction Kit LIGHT-BOOK · MAUDE
#313 of 1000 · 5,152 reports · 1992–2026
- BOOK 5,152 reports
- RANK #313 of 1000
- DEATH 5 death-typed
- INJ 1,352 injury-typed
- MALF 3,556 malfunction
- SPAN 1992–2026
- PEAK 2019: 472
- PHOTO Tissue Expander And A…
Nearest event-volume peer: Tissue Expander And Accessories (4 report gap)
Anesthesia Conduction Kit sits #313 of 1000 among tracked device types with 5,152 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 →
Malfunction reports run above the device-type norm
Anesthesia Conduction Kit carries 69.0% MALFUNCTION-coded reports, 4.2pp 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 26.2% corpus 30.3% · below corpus mean (-4.1 pp)
- MALF 69.0% corpus 64.8% · above corpus mean (+4.2 pp)
Lead product-problem code Break is 22% of coded problems · Lead manufacturer ARROW INTERNATIONAL INC. accounts for 32% of manufacturer-tagged reports · Top event location is 41% of location-tagged rows .
Anesthesia Conduction Kit in the event-volume neighbourhood
FDA MAUDE report totals among this device type and nearest nationwide peers
- Light
Light, Surgical, Ceiling Mounted
5,203 reports
- Prosthesis
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
5,172 reports
- Anesthesia Co… (this)
Anesthesia Conduction Kit
5,152 reports
- Tissue Expand…
Tissue Expander And Accessories
5,148 reports
- Prosthesis
Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing
5,146 reports
- Accessories
Accessories, Arthroscopic
5,126 reports
What this shows Anesthesia Conduction Kit carries 5,152 MAUDE reports, ranked #313 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 (138) held close to the prior two-year average of 113.
Related Entities for Anesthesia Conduction Kit
Top Manufacturers
Event Locations
Compare ARROW INTERNATIONAL INC. vs SMITHS MEDICAL ASD, INC. →
Nationwide devices with a comparable volume-and-death footprint
Two openFDA-derived peer sets for Anesthesia Conduction Kit: 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 (5,152 here).
Similar death-typed counts
Nearest other device types by death-typed report count (5 here), distinct from the volume row.
Read our methodology - how this data is sourced, computed, and verified.
Disclaimer: MAUDE figures for Anesthesia Conduction Kit 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 Anesthesia Conduction Kit; 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.