MEDTRONIC PUERTO RICO OPERATIONS MED-REL
Manufacturer adverse-event records for MEDTRONIC PUERTO RICO OPERATIONS MED-REL 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 · 2006–2011 · mid-book · elevated Death-code · injury-heavy
Death-code intensity
MEDTRONIC PUERTO RICO OPERATIONS MED-REL carries an elevated Death-code share
Death-coded event_type rows are 239 of 10,677 (2.24% · elevated tercile among 443 manufacturers). Absolute volume is mid-book.
What the Death-code reading shows for MEDTRONIC PUERTO RICO OPERATIONS MED-REL
The standout signal for MEDTRONIC PUERTO RICO OPERATIONS MED-REL is Death-code intensity: 2.24% of 10,677 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 PUERTO RICO OPERATIONS MED-REL. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.
Reports span 10 device types, led in this extract by Injury at 6,387 (59.8% of event_type total). Peak single-year volume reaches 3,586 reports across 6 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 (10)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.