DEDevice Outcomes Registry
Adverse event

YELLOFINS STIRRUP

ALLEN MEDICAL SYSTEMS, INC. device event report from FDA MAUDE/openFDA; review identifiers and clinical context before acting.

What this profile means

This public preview summarizes the normalized record without exposing paid citation paths. Use it to decide whether the device deserves a paid report, workspace review, or direct source verification.

Record typedevice
CategoryAdverse event
StatusMalfunction
Confidence90
FDA record typeAdverse event
ManufacturerALLEN MEDICAL SYSTEMS, INC.
Device/modelYELLOFINS STIRRUP
Event typeMalfunction
FDA class/statusMalfunction

Source coverage preview

Public pages show source names and record counts. Paid reports unlock source URLs, citation paths, and report-generation context.

Source rows checked2
Max source confidence90
Latest source observationMay 18, 2026
CitationsLocked in paid report
  • openFDA Device Adverse Events

Paid report value

  • Device or manufacturer signal snapshot
  • Recall/adverse-event interpretation and clinical review checklist
  • Source citations and source-observed dates
  • Questions for clinicians, compliance teams, or counsel

For records that need deeper review, use the main access flow to request source-backed report context, saved workspace review, or support before relying on the public preview.

Methodology and limits

Source-backed, but still worth verifying for high-impact use.

Medical-device data is source-backed intelligence for review. It is not a diagnosis, clinical recommendation, or proof of causation.

For patients

Understand what a public signal does and does not prove.

For clinicians

Use reports for inventory or chart review triage.

For compliance

Monitor model and manufacturer signals over time.

Questions to ask before relying on this record

Paid reports include citation paths and report-generation context; public previews intentionally hide source URLs.

YELLOFINS STIRRUP Adverse event Report | DataVerityHub