Device: Endotracheal Tube
51 adverse event reports submitted to the FDA
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
390.0%
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%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.