MEDTRONIC S.A.
Manufacturer adverse-event records for MEDTRONIC S.A. 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 · 2000–2016 · mid-book · elevated Death-code · injury-heavy
Death-code intensity
MEDTRONIC S.A. carries an elevated Death-code share
Death-coded event_type rows are 446 of 10,690 (4.17% · elevated tercile among 434 manufacturers). Absolute volume is mid-book.
What the Death-code reading shows for MEDTRONIC S.A.
The standout signal for MEDTRONIC S.A. is Death-code intensity: 4.17% of 10,690 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 MEDTRONIC S.A.. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.
Reports span 13 device types, led in this extract by Injury at 7,924 (74.1% of event_type total). Peak single-year volume reaches 2,805 reports across 17 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 (13)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.