Device: Collection, Blood
13 adverse event reports submitted to the FDA
Active Ingredients
Administration Routes
Species Affected
Most Affected Breeds
Most Reported Reactions
Outcome Breakdown
Data Summary
| Metric | Value |
|---|---|
| Total adverse event reports | 13 |
| Reports involving death | 1 |
| Case-fatality rate (reported events) | 770.0% |
| Distinct species in reports | 3 |
| Distinct breeds in reports | 2 |
| Distinct reactions reported | 7 |
| Active ingredients on file | 1 |
Source: FDA Center for Veterinary Medicine — Adverse Event Reporting (CVM AER). Counts reflect voluntary reports only.
Device: Collection, Blood Adverse Event Insights
The FDA Center for Veterinary Medicine database currently holds 13 adverse event reports referencing Device: Collection, Blood, including 1 reports in which the animal died — a 770.0% case-fatality figure among reported events only, not a population-level mortality rate. Active ingredient on file: Device: Collection, Blood. Reported administration route is Unknown. These numbers reflect voluntary submissions from pet owners, veterinarians, and manufacturers and therefore under-represent mild events and over-represent severe ones — a pattern the FDA has documented repeatedly for pharmacovigilance datasets.
The species most frequently named in Device: Collection, Blood reports are Unknown (11 reports), Primate (1 reports), Dog (1 reports), with Unknown accounting for the largest share. Within those species, Unknown (12), Primate (unknown) (1) appear most often — though breed popularity and ownership density shape these counts as much as any drug-specific sensitivity. This distribution matters because the same active ingredient can behave very differently across body sizes, ages, and species physiology.
The most commonly reported clinical signs associated with Device: Collection, Blood are Device Defective NOS (13), Death (1), Disseminated intravascular coagulation (1), Acute renal failure (1). Of the 2 reports with a coded outcome, Died is the leading category at 50.0%. Because FDA adverse event data describes correlation rather than causation, these figures are best used to frame informed questions with a veterinarian and to compare reporting patterns across related products — not as a standalone safety verdict on Device: Collection, Blood.
Source: FDA Center for Veterinary Medicine — Adverse Event Reports FDA Center for Veterinary Medicine — Adverse Event Reports Data reflects voluntary submissions and may not represent actual incidence rates
Read our methodology — how this data is sourced, computed, and verified.