Device: Intracardiac/Intravascular Surgical Catheters
23 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.
23
Total Reports
5
Deaths Reported
2170.0%
Death Rate
Active Ingredients
Device: Intracardiac/Intravascular Surgical Catheters
Administration Routes
UnknownIntravenous
Species Affected
Unknown 14
Pig 5
Dog 2
Other 1
Cat 1
Most Affected Breeds
Unknown 15
Pig (unknown) 4
Dog (unknown) 2
Yorkshire (Pig) also known as American Yorkshire 1
Cat (unknown) 1
Most Reported Reactions
Device Defective NOS 8
Product Defect, General 4
Ulceration NOS 2
Death by euthanasia 2
PR-HEART, LESION(S) 2
Death 2
Complications of device insertion 2
Device Complication NOS 2
Vascular disorder NOS (see also endocarditis) 2
Device failure 2
Application site reaction NOS 1
Injury associated with device 1
Outcome Breakdown
Died
4 (44.4%)
Outcome Unknown
4 (44.4%)
Euthanized
1 (11.1%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.