DEPUY ORTHOPAEDICS, INC. 1818910
Manufacturer adverse-event records for DEPUY ORTHOPAEDICS, INC. 1818910 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 · 2005–2023 · heavy-book · typical Death-code · injury-heavy
Injury-mix signature
DEPUY ORTHOPAEDICS, INC. 1818910 leans injury-heavy in event_type mix
Injury-coded event_type share is 69.8% (injury-heavy tercile) beside 0.09% Death-coded (typical). Volume band: heavy.
What the Injury-mix reading shows for DEPUY ORTHOPAEDICS, INC. 1818910
The standout signal for DEPUY ORTHOPAEDICS, INC. 1818910 is Injury-mix: 69.8% Injury-coded (injury-heavy) beside 0.09% Death-coded, on a heavy-book footprint.
As a heavy-book manufacturer, portfolio size and reporting obligations inflate absolute counts - pair DEPUY ORTHOPAEDICS, INC. 1818910 with device-family pages before treating company totals as a safety verdict. Event_type Death and Injury are one code per report; Patient Outcomes below use a separate FDA population.
Reports span 20 device types, led in this extract by Injury at 24,619 (69.8% of event_type total). Peak single-year volume reaches 9,424 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.