Reaction profile
The FDA adverse-event record for complications of device insertion
17 FDA adverse-event reports reference complications of device insertion (VeDDRA 93023). See the species, breeds, and drugs most associated with it below.
- 17
- reports citing this reaction
- 5.9%
- death-coded share
- Unknown
- most-affected species
- Device: Surgical Instruments
- most-associated drug
Species Most Affected
Breeds Most Affected
Associated Drugs
Complications of device insertion Reaction Insights
17 reports name Complications of device insertion; 1 recorded a death outcome (5.9% of reported events, not a population-level mortality rate). VeDDRA code: 93023.
By species: Unknown (8 reports), Dog (6 reports), Pig (1 reports). By breed: Unknown (10), Dog (unknown) (4), Pig (unknown) (1).
Most co-reported drugs: Device: Surgical Instruments (8 reports), Device: Suture (3 reports), Device: Intracardiac/Intravascular Surgical Catheters (2 reports), Device: Syringe (2 reports).
Read these counts as reporting volume, not risk: per our methodology, co-reporting reflects temporal association captured in voluntary submissions, not proof that a drug caused this reaction. A widely-prescribed drug will rack up more raw co-reports at an identical true rate than a rarely-used one, so compare within similar-exposure products.
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.