COVIDIEN MFG DC BOULDER
Manufacturer adverse-event records for COVIDIEN MFG DC BOULDER come from the U.S. Food & Drug Administration (FDA) MAUDE database via openFDA, refreshed March 2026 - see our methodology. Not medical advice.
FDA MAUDE device safety record · 2017–2025 · mid-book · typical Death-code · balanced
Death-code intensity
COVIDIEN MFG DC BOULDER tracks a typical Death-code share
Death-coded event_type rows are 82 of 14,148 (0.58% · typical tercile among 434 manufacturers). Absolute volume is mid-book.
What the Death-code reading shows for COVIDIEN MFG DC BOULDER
The standout signal for COVIDIEN MFG DC BOULDER is Death-code intensity: 0.58% of 14,148 reports (typical tercile), while absolute volume is mid-book.
Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for COVIDIEN MFG DC BOULDER. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.
Reports span 20 device types, led in this extract by Malfunction at 12,517 (88.5% of event_type total). Peak single-year volume reaches 2,274 reports across 9 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.
Event Types
Patient Outcomes
FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.
Devices (20)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.