2026 data FDA MAUDE openFDA

Display, Cathode-Ray Tube, Medical

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 Display, Cathode-Ray Tube, Medical LIGHT-BOOK · MAUDE

#880 of 1000 · 491 reports · 2001–2026

  • BOOK 491 reports
  • RANK #880 of 1000
  • DEATH 14 death-typed
  • INJ 20 injury-typed
  • MALF 454 malfunction
  • SPAN 2001–2026
  • PEAK 2010: 147
  • PHOTO Glue

Nearest event-volume peer: Glue, Surgical, Arteries (1 report gap)

Display, Cathode-Ray Tube, Medical sits #880 of 1000 among tracked device types with 491 MAUDE reports spanning 2001–2026. 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 2.9% corpus 1.5% · above corpus mean (+1.3 pp)
  • INJ 4.1% corpus 30.4% · below corpus mean (-26.4 pp)
  • MALF 92.5% corpus 64.5% · above corpus mean (+28.0 pp)

Lead product-problem code No Display/Image is 15% of coded problems · Lead manufacturer MERIT MEDICAL SYSTEMS, INC. accounts for 62% of manufacturer-tagged reports · Top event location is 80% of location-tagged rows .

Display, Cathode-Ray Tube, Medical in the event-volume neighbourhood

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

reports

What this shows Display, Cathode-Ray Tube, Medical carries 491 MAUDE reports, ranked #880 of 1000.

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

Event Types

Malfunction 454 (92.5%)
Injury 20 (4.1%)
Death 14 (2.9%)
Other 2 (0.4%)
1 (0.2%)

Patient Outcomes

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

439 (88.5%)
Other 28 (5.6%)
Death 14 (2.8%)
Required Intervention 6 (1.2%)
O 3 (0.6%)
Life Threatening 3 (0.6%)
L 1 (0.2%)
R 1 (0.2%)
Hospitalization 1 (0.2%)

Top Product Problems

No Display/Image 13
Data Problem 8
Application Program Problem: Medication Error 7
Computer Operating System Problem 7
No Audible Alarm 7
Appropriate Term/Code Not Available 4
Incorrect, Inadequate or Imprecise Result or Readings 4
Output Problem 4
Device Alarm System 3
Display or Visual Feedback Problem 3
Erratic or Intermittent Display 3
Inaccurate Delivery 3
No Device Output 3
Patient Data Problem 3
Adverse Event Without Identified Device or Use Problem 2
Defective Device 2
Device Operates Differently Than Expected 2
Device Packaging Compromised 2
Failure to Transmit Record 2
Improper or Incorrect Procedure or Method 2

Yearly Trend

01
2001: 1
03
2003: 1
04
2004: 7
05
2005: 1
07
2007: 3
08
2008: 5
09
2009: 29
10
2010: 147
11
2011: 129
12
2012: 21
13
2013: 4
14
2014: 13
15
2015: 15
16
2016: 7
17
2017: 10
18
2018: 3
19
2019: 29
20
2020: 22
21
2021: 6
22
2022: 2
23
2023: 17
24
2024: 15
25
2025: 3
26
2026: 1

Related Entities for Display, Cathode-Ray Tube, Medical

Event Locations

393 (80.0%)
I 90 (18.3%)
HOSPITAL 5 (1.0%)
NO INFORMATION 3 (0.6%)

Compare MERIT MEDICAL SYSTEMS, INC. vs PHILIPS MEDICAL SYSTEMS →

Nationwide devices with similar MAUDE profiles

Two openFDA-derived peer sets for Display, Cathode-Ray Tube, Medical, 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 (491 here).

Similar death-typed counts

Nearest other device types by death-typed report count (14 here), distinct from the volume row.

Disclaimer: MAUDE figures for Display, Cathode-Ray Tube, Medical 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 Display, Cathode-Ray Tube, Medical; 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.