DEPUY INTL., LTD. - 8010379

Manufacturer adverse-event records for DEPUY INTL., LTD. - 8010379 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 · 2010–2015 · thin-book · typical Death-code · injury-heavy

Injury-mix signature

DEPUY INTL., LTD. - 8010379 leans injury-heavy in event_type mix

Injury-coded event_type share is 97.6% (injury-heavy tercile) beside 0.20% Death-coded (typical). Volume band: thin.

What the Injury-mix reading shows for DEPUY INTL., LTD. - 8010379

The standout signal for DEPUY INTL., LTD. - 8010379 is Injury-mix: 97.6% Injury-coded (injury-heavy) beside 0.20% Death-coded, on a thin-book footprint.

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 14 device types, led in this extract by Injury at 6,505 (97.6% of event_type total). Peak single-year volume reaches 3,792 reports across 6 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

6,664
Total Reports
13
Event-type Death
6,505
Injury Reports
14
Device Types

Event Types

Injury 6,505 (97.6%)
Malfunction 143 (2.1%)
Death 13 (0.2%)
3 (0.0%)

Patient Outcomes

FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.

Required Intervention 4,355 (63.0%)
Other 2,130 (30.8%)
R 243 (3.5%)
162 (2.3%)
Death 16 (0.2%)
O 2 (0.0%)
Congenital Anomaly 1 (0.0%)

Yearly Trend

10
2010: 2
11
2011: 26
12
2012: 76
13
2013: 3,792
14
2014: 1,181
15
2015: 1,587