Depuy International Ltd - 8010379
FDA adverse event reports naming Depuy International Ltd - 8010379 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY INTERNATIONAL LTD - 8010379.
- Total reports
- 12,615
- Deaths
- 45
- Injuries
- 10,631
- Malfunctions
- 1,939
Reports per year
46412
51113
25814
1,52015
19316
50417
1,21418
1,46419
1,67320
1,35021
1,11122
1,15523
65824
21025
6726
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA6,036
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI1,902
- Prosthesis, Hip, Femoral, ResurfacingKXA974
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH762
- Driver, ProsthesisHWR593
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY524
- ReamerHTO266
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL204
- ImpactorHWA199
- TemplateHWT139
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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