2026 data FDA MAUDE openFDA FDA Class II

Endoscope Channel Accessory

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 §876.1500 (Gastroenterology, Urology panel).

FDA MAUDE casebook

openFDA event book Endoscope Channel Accessory LIGHT-BOOK · MAUDE

#793 of 1000 · 666 reports · 2012–2026

  • BOOK 666 reports
  • RANK #793 of 1000
  • DEATH 0 death-typed
  • INJ 36 injury-typed
  • MALF 623 malfunction
  • SPAN 2012–2026
  • PEAK 2026: 205
  • PHOTO Accessories

Nearest event-volume peer: Accessories, Cleaning Brushes, For Endoscope (2 report gap)

Endoscope Channel Accessory sits #793 of 1000 among tracked device types with 666 MAUDE reports spanning 2012–2026. 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

Endoscope Channel Accessory carries 93.5% MALFUNCTION-coded reports, 28.7pp above the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.

  • DEATH 0.0% corpus 1.5% · below corpus mean (-1.5 pp)
  • INJ 5.4% corpus 30.3% · below corpus mean (-24.9 pp)
  • MALF 93.5% corpus 64.8% · above corpus mean (+28.7 pp)

Lead product-problem code Detachment of Device or Device Component is 24% of coded problems · Lead manufacturer BOSTON SCIENTIFIC CORPORATION accounts for 95% of manufacturer-tagged reports · Top event location is 71% of location-tagged rows .

Endoscope Channel Accessory in the event-volume neighbourhood

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

reports

What this shows Endoscope Channel Accessory carries 666 MAUDE reports, ranked #793 of 1000.

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

Event Types

Malfunction 623 (93.5%)
Injury 36 (5.4%)
7 (1.1%)

Patient Outcomes

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

595 (93.8%)
Required Intervention 24 (3.8%)
Other 11 (1.7%)
Hospitalization 4 (0.6%)

Top Product Problems

Detachment of Device or Device Component 227
Physical Resistance/Sticking 146
Leak/Splash 107
Fluid/Blood Leak 105
Suction Problem 58
Infusion or Flow Problem 51
Use of Device Problem 51
Adverse Event Without Identified Device or Use Problem 24
Material Integrity Problem 24
Break 19
Defective Device 16
Difficult or Delayed Positioning 16
Difficult to Remove 15
Device Dislodged or Dislocated 14
Material Separation 13
Device Slipped 12
Insufficient Device Problem Information 10
Difficult to Advance 8
Difficult to Insert 8
Entrapment of Device 8

Yearly Trend

12
2012: 1
13
2013: 1
14
2014: 2
15
2015: 3
16
2016: 8
17
2017: 12
18
2018: 17
19
2019: 40
20
2020: 54
21
2021: 52
22
2022: 37
23
2023: 43
24
2024: 100
25
2025: 91
26
2026: 205

Reports in 2025 (91) held close to the prior two-year average of 72.

Related Entities for Endoscope Channel Accessory

Event Locations

476 (71.5%)
I 145 (21.8%)
HOSPITAL 35 (5.3%)
NO INFORMATION 8 (1.2%)
OTHER 1 (0.2%)
OUTPATIENT TREATMENT FACILITY 1 (0.2%)

Compare BOSTON SCIENTIFIC CORPORATION vs WILSON-COOK MEDICAL INC →

Nationwide devices with a comparable report-volume footprint

Endoscope Channel Accessory carries zero death-typed MAUDE reports, so the peer set below compares report volume only; both axes are floored at ≥100 reports so the neighborhood stays in the advertised mass.

Similar report volume

Nearest other device types by FDA MAUDE report count (666 here).

Similar death-typed counts

Nearest other device types by death-typed report count (0 here), distinct from the volume row.

Disclaimer: MAUDE figures for Endoscope Channel Accessory 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 Endoscope Channel Accessory; 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.