Drug profile

The FDA adverse-event record for Device: Endotracheal Tube

51 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Device: Endotracheal Tube. See the species affected, top reactions, and outcomes below.

51
adverse-event reports
3.9%
death-coded share
Unknown
most-reported species
16
Lack of efficacy, medical device - top reaction
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Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
51
Total Reports
2
Deaths Reported
3.9%
Death Rate

Active Ingredients

Device: Endotracheal Tube

Administration Routes

Unknown

Species Affected

Unknown 49
Dog 1
Other 1

Most Affected Breeds

Unknown 50
Dog (unknown) 1

Most Reported Reactions

Lack of efficacy, medical device 16
Device failure 16
Device Defective NOS 15
Product Defect, General 11
Broken components, medical device 8
Death 2
Cyanosis 2
Bradycardia 1
Systemic disorder NOS 1
Device breakage/fracture 1
Laboured breathing 1
Respiratory arrest 1

Outcome Breakdown

Died
2 (66.7%)
Recovered/Normal
1 (33.3%)

Device: Endotracheal Tube Adverse Event Insights

51 reports name Device: Endotracheal Tube; 2 recorded a death outcome (3.9% of reported events, not a population-level mortality rate). Active ingredient: Device: Endotracheal Tube. Administration route: Unknown.

By species: Unknown (49 reports), Dog (1 reports), Other (1 reports). By breed: Unknown (50), Dog (unknown) (1).

Leading clinical signs: Lack of efficacy, medical device (16), Device failure (16), Device Defective NOS (15), Product Defect, General (11). Outcome, 3 coded reports: Died leads at 66.7%.

Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.