1818910 DEPUY ORTHOPAEDICS, INC.

Manufacturer adverse-event records for 1818910 DEPUY ORTHOPAEDICS, INC. 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 · 2010–2017 · thin-book · quiet Death-code · injury-heavy

Injury-mix signature

1818910 DEPUY ORTHOPAEDICS, INC. leans injury-heavy in event_type mix

Injury-coded event_type share is 94.1% (injury-heavy tercile) beside 0.02% Death-coded (quiet). Volume band: thin.

What the Injury-mix reading shows for 1818910 DEPUY ORTHOPAEDICS, INC.

The standout signal for 1818910 DEPUY ORTHOPAEDICS, INC. is Injury-mix: 94.1% Injury-coded (injury-heavy) beside 0.02% 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 20 device types, led in this extract by Injury at 5,594 (94.1% of event_type total). Peak single-year volume reaches 4,282 reports across 8 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

5,947
Total Reports
1
Event-type Death
5,594
Injury Reports
20
Device Types

Event Types

Injury 5,594 (94.1%)
Malfunction 352 (5.9%)
Death 1 (0.0%)

Patient Outcomes

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

Required Intervention 5,617 (94.4%)
278 (4.7%)
Other 51 (0.9%)
R 1 (0.0%)
Death 1 (0.0%)

Yearly Trend

10
2010: 1
11
2011: 4
12
2012: 7
13
2013: 4,282
14
2014: 1,078
15
2015: 75
16
2016: 477
17
2017: 23