2026 data FDA MAUDE openFDA FDA Class III

Glue, Surgical, Arteries

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 Glue, Surgical, Arteries LIGHT-BOOK · MAUDE

#895 of 1000 · 495 reports · 2003–2026

  • BOOK 495 reports
  • RANK #895 of 1000
  • DEATH 45 death-typed
  • INJ 420 injury-typed
  • MALF 8 malfunction
  • SPAN 2003–2026
  • PEAK 2015: 56
  • PHOTO Angiography/Angioplas…

Nearest event-volume peer: Angiography/Angioplasty Kit (1 report gap)

Glue, Surgical, Arteries sits #895 of 1000 among tracked device types with 495 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 →

Malfunction reports sit below the device-type norm

Glue, Surgical, Arteries carries 1.6% MALFUNCTION-coded reports, 63.2pp below the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.

  • DEATH 9.1% corpus 1.5% · above corpus mean (+7.6 pp)
  • INJ 84.8% corpus 30.3% · above corpus mean (+54.6 pp)
  • MALF 1.6% corpus 64.8% · below corpus mean (-63.2 pp)

Lead product-problem code Adverse Event Without Identified Device or Use Problem is 42% of coded problems · Lead manufacturer UNK accounts for 100% of manufacturer-tagged reports · Top event location is 56% of location-tagged rows .

Glue, Surgical, Arteries in the event-volume neighbourhood

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

reports

What this shows Glue, Surgical, Arteries carries 495 MAUDE reports, ranked #895 of 1000.

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

Event Types

Injury 420 (84.8%)
Death 45 (9.1%)
13 (2.6%)
Other 9 (1.8%)
Malfunction 8 (1.6%)

Patient Outcomes

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

Other 285 (42.4%)
O 75 (11.2%)
R 61 (9.1%)
Hospitalization 61 (9.1%)
Required Intervention 50 (7.4%)
Death 47 (7.0%)
Life Threatening 36 (5.4%)
L 24 (3.6%)
14 (2.1%)
H 10 (1.5%)
S 7 (1.0%)
D 1 (0.1%)
Disability 1 (0.1%)

Top Product Problems

Adverse Event Without Identified Device or Use Problem 214
Insufficient Device Problem Information 141
Appropriate Device Problem Term/Code Not Available 29
Improper or Incorrect Procedure or Method 25
Device Operates Differently Than Expected 20
Failure To Adhere Or Bond 10
Patient-Device Incompatibility 10
Migration or Expulsion of Device 9
Material Fragmentation 7
Off-Label Use 7
Loss of or Failure to Bond 6
Material Integrity Problem 5
Contamination 4
Use of Device Problem 4
Material Disintegration 3
Material Separation 3
Migration 3
Peeled/Delaminated 3
Biocompatibility 2
Break 2

Yearly Trend

03
2003: 2
04
2004: 1
09
2009: 14
10
2010: 50
11
2011: 29
12
2012: 33
13
2013: 46
14
2014: 40
15
2015: 56
16
2016: 28
17
2017: 31
18
2018: 25
19
2019: 39
20
2020: 25
21
2021: 25
22
2022: 12
23
2023: 7
24
2024: 14
25
2025: 11
26
2026: 7

Reports in 2025 (11) held close to the prior two-year average of 11.

Related Entities for Glue, Surgical, Arteries

Top Manufacturers

UNK 2

Event Locations

278 (56.2%)
I 207 (41.8%)
HOSPITAL 7 (1.4%)
NO INFORMATION 3 (0.6%)

Nationwide devices with a comparable volume-and-death footprint

Two openFDA-derived peer sets for Glue, Surgical, Arteries: 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 (495 here).

Similar death-typed counts

Nearest other device types by death-typed report count (45 here), distinct from the volume row.

Disclaimer: MAUDE figures for Glue, Surgical, Arteries 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 Glue, Surgical, Arteries; 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.