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2026 data FDA MAUDE openFDA

Absorbable Coronary Drug-Eluting Stent

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.

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FDA MAUDE casebook

openFDA event book Absorbable Coronary Drug-Eluting Stent LIGHT-BOOK · MAUDE

#672 of 1000 · 929 reports · 2016–2026

  • BOOK 929 reports
  • RANK #672 of 1000
  • DEATH 110 death-typed
  • INJ 784 injury-typed
  • MALF 35 malfunction
  • SPAN 2016–2026
  • PEAK 2017: 328
  • PHOTO Resectoscope

Nearest event-volume peer: Resectoscope (9 report gap)

Absorbable Coronary Drug-Eluting Stent sits #672 of 1000 among tracked device types with 929 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 →

Event-type mix vs corpus

Shares of FDA event_type codes on this device type, compared with the mean across 1,000 device types that have ≥100 MAUDE reports. Codes are report labels, not adjudicated causation.

  • DEATH 11.8% corpus 1.5% · above corpus mean (+10.3 pp)
  • INJ 84.4% corpus 30.4% · above corpus mean (+54.0 pp)
  • MALF 3.8% corpus 64.5% · below corpus mean (-60.7 pp)

Lead product-problem code Adverse Event Without Identified Device or Use Problem is 82% of coded problems · Lead manufacturer AV-TEMECULA-CT accounts for 72% of manufacturer-tagged reports · Top event location I is 95% of location-tagged rows .

Absorbable Coronary Drug-Eluting Stent in the event-volume neighbourhood

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

reports

What this shows Absorbable Coronary Drug-Eluting Stent carries 929 MAUDE reports, ranked #672 of 1000.

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

Event Types

Injury 784 (84.4%)
Death 110 (11.8%)
Malfunction 35 (3.8%)

Patient Outcomes

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

Hospitalization 627 (33.5%)
R 610 (32.6%)
S 305 (16.3%)
Death 109 (5.8%)
Required Intervention 100 (5.4%)
Other 51 (2.7%)
34 (1.8%)
H 11 (0.6%)
L 10 (0.5%)
O 6 (0.3%)
Life Threatening 4 (0.2%)
D 1 (0.1%)
Disability 1 (0.1%)

Top Product Problems

Adverse Event Without Identified Device or Use Problem 810
Improper or Incorrect Procedure or Method 42
Patient-Device Incompatibility 27
Difficult or Delayed Positioning 26
Break 10
Detachment Of Device Component 9
Device Operates Differently Than Expected 6
Difficult To Position 6
Difficult or Delayed Activation 6
Failure to Advance 6
Material Rupture 6
Positioning Failure 5
Difficult to Remove 4
Material Deformation 4
Physical Resistance 4
Inflation Problem 3
Off-Label Use 3
Product Quality Problem 3
Device Damaged by Another Device 2
Device Expiration Issue 2

Yearly Trend

16
2016: 224
17
2017: 328
18
2018: 105
19
2019: 38
20
2020: 168
21
2021: 23
22
2022: 7
23
2023: 10
24
2024: 4
25
2025: 16
26
2026: 6

Related Entities for Absorbable Coronary Drug-Eluting Stent

Top Manufacturers

AV-TEMECULA-CT 672
ABBOTT VASCULAR 255
ABBOTT 1

Event Locations

I 881 (94.8%)
44 (4.7%)
NO INFORMATION 3 (0.3%)
HOSPITAL 1 (0.1%)

Compare AV-TEMECULA-CT vs ABBOTT VASCULAR →

Nationwide devices with similar MAUDE profiles

Two openFDA-derived peer sets for Absorbable Coronary Drug-Eluting Stent, both floored at ≥100 reports so the neighborhoods stay in the advertised mass.

Similar report volume

Nearest other device types by FDA MAUDE report count (929 here).

Resectoscope 920 Midline Catheter 939 System, X-Ray, Mobile 913 Bed, Manual 912

Similar death-typed counts

Nearest other device types by death-typed report count (110 here), distinct from the volume row.

Extractor, Vacuum, Fetal 111 Temporary Carotid Catheter For Embolic Capt… 109 Rod 112 Gas-Machine, Anesthesia 107

Read our methodology - how this data is sourced, computed, and verified.

Disclaimer: MAUDE figures for Absorbable Coronary Drug-Eluting Stent 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 Absorbable Coronary Drug-Eluting Stent; 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.