CORDIS DE MEXICO
Manufacturer adverse-event records for CORDIS DE MEXICO 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 · 2002–2021 · mid-book · elevated Death-code · injury-heavy
Death-code intensity
CORDIS DE MEXICO carries an elevated Death-code share
Death-coded event_type rows are 1,121 of 15,476 (7.24% · elevated tercile among 443 manufacturers). Absolute volume is mid-book.
What the Death-code reading shows for CORDIS DE MEXICO
The standout signal for CORDIS DE MEXICO is Death-code intensity: 7.24% of 15,476 reports (elevated tercile), while absolute volume is mid-book.
Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for CORDIS DE MEXICO. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.
Reports span 20 device types, led in this extract by Injury at 8,887 (57.4% of event_type total). Peak single-year volume reaches 2,759 reports across 19 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.