BIOMET 3I
Manufacturer adverse-event records for BIOMET 3I 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 · 2007–2025 · mid-book · quiet Death-code · injury-heavy
Death-code intensity
BIOMET 3I is quieter on Death-coded events
Death-coded event_type rows are 0 of 18,760 (0.00% · quiet tercile among 434 manufacturers). Absolute volume is mid-book.
What the Death-code reading shows for BIOMET 3I
The standout signal for BIOMET 3I is Death-code intensity: 0.00% of 18,760 reports (quiet tercile), while absolute volume is mid-book.
Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for BIOMET 3I. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.
Reports span 20 device types, led in this extract by Injury at 12,395 (66.1% of event_type total). Peak single-year volume reaches 3,034 reports across 18 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.