2026 data FDA MAUDE openFDA

Cannula, Nasal, Oxygen

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 Cannula, Nasal, Oxygen LIGHT-BOOK · MAUDE

#515 of 1000 · 1,730 reports · 1992–2026

  • BOOK 1,730 reports
  • RANK #515 of 1000
  • DEATH 30 death-typed
  • INJ 197 injury-typed
  • MALF 1,441 malfunction
  • SPAN 1992–2026
  • PEAK 2016: 174
  • PHOTO Cannula

Nearest event-volume peer: Cannula, Manipulator/Injector, Uterine (7 report gap)

Cannula, Nasal, Oxygen sits #515 of 1000 among tracked device types with 1,730 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 →

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 1.7% corpus 1.5% · near corpus mean (+0.2 pp)
  • INJ 11.4% corpus 30.4% · below corpus mean (-19.1 pp)
  • MALF 83.3% corpus 64.5% · above corpus mean (+18.8 pp)

Lead product-problem code Break is 23% of coded problems · Lead manufacturer FISHER & PAYKEL HEALTHCARE LTD accounts for 76% of manufacturer-tagged reports · Top event location is 48% of location-tagged rows .

Cannula, Nasal, Oxygen in the event-volume neighbourhood

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

reports

What this shows Cannula, Nasal, Oxygen carries 1,730 MAUDE reports, ranked #515 of 1000.

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

Event Types

Malfunction 1,441 (83.3%)
Injury 197 (11.4%)
Other 37 (2.1%)
Death 30 (1.7%)
25 (1.4%)

Patient Outcomes

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

1,404 (79.9%)
Other 168 (9.6%)
Required Intervention 78 (4.4%)
Death 31 (1.8%)
Hospitalization 23 (1.3%)
Life Threatening 19 (1.1%)
R 15 (0.9%)
O 8 (0.5%)
Disability 6 (0.3%)
S 3 (0.2%)
H 2 (0.1%)
L 1 (0.1%)

Top Product Problems

Break 255
Detachment of Device or Device Component 177
Device Handling Problem 118
Material Split, Cut or Torn 99
Device Issue 82
Disconnection 66
Use of Device Problem 36
Hole In Material 35
Split 35
Material Separation 27
Material Integrity Problem 25
Connection Problem 22
Leak/Splash 21
Adverse Event Without Identified Device or Use Problem 19
Gas/Air Leak 18
Kinked 17
Loose or Intermittent Connection 16
Material Twisted/Bent 16
Obstruction of Flow 16
Patient Device Interaction Problem 14

Yearly Trend

92
1992: 2
93
1993: 2
94
1994: 5
95
1995: 5
96
1996: 12
97
1997: 3
98
1998: 4
00
2000: 3
01
2001: 9
02
2002: 6
03
2003: 5
04
2004: 3
05
2005: 8
06
2006: 5
07
2007: 8
08
2008: 12
09
2009: 19
10
2010: 44
11
2011: 33
12
2012: 50
13
2013: 118
14
2014: 147
15
2015: 109
16
2016: 174
17
2017: 128
18
2018: 91
19
2019: 105
20
2020: 135
21
2021: 128
22
2022: 74
23
2023: 116
24
2024: 75
25
2025: 81
26
2026: 11

Related Entities for Cannula, Nasal, Oxygen

Event Locations

830 (48.0%)
I 732 (42.3%)
HOSPITAL 107 (6.2%)
NO INFORMATION 27 (1.6%)
HOME 19 (1.1%)
INVALID DATA 6 (0.3%)
UNKNOWN 3 (0.2%)
NOT APPLICABLE 2 (0.1%)
OTHER 2 (0.1%)
NURSING HOME 1 (0.1%)
OUTPATIENT TREATMENT FACILITY 1 (0.1%)

Compare FISHER & PAYKEL HEALTHCARE LTD vs TELEFLEX MEDICAL →

Nationwide devices with similar MAUDE profiles

Two openFDA-derived peer sets for Cannula, Nasal, Oxygen, 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 (1,730 here).

Similar death-typed counts

Nearest other device types by death-typed report count (30 here), distinct from the volume row.

Disclaimer: MAUDE figures for Cannula, Nasal, Oxygen 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 Cannula, Nasal, Oxygen; 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.