DEPUY FRANCE SAS - 3003895575
Manufacturer adverse-event records for DEPUY FRANCE SAS - 3003895575 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 · 2010–2026 · thin-book · typical Death-code · injury-heavy
Volume signature
DEPUY FRANCE SAS - 3003895575 is a thinner MAUDE footprint
DEPUY FRANCE SAS - 3003895575 accounts for 4,881 FDA MAUDE reports (#379 of 434, thin-book tercile). Death-coded event_type share is 0.14% (typical); Injury share 63.7% (injury-heavy).
What the volume reading shows for DEPUY FRANCE SAS - 3003895575
The standout signal for DEPUY FRANCE SAS - 3003895575 is filing volume: 4,881 adverse-event reports in FDA MAUDE (#379 of 434, thin-book). Death-coded event_type share sits at 0.14% (typical).
As a thinner-book manufacturer, a handful of device families can swing the totals; open the device table rather than reading the company headline alone. Event_type counts are not the same population as Patient Outcomes.
Reports span 20 device types, led in this extract by Injury at 3,111 (63.7% of event_type total). Peak single-year volume reaches 1,110 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 (20)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.