Depuy Intl., Ltd. - 8010379
FDA adverse event reports naming Depuy Intl., Ltd. - 8010379 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY INTL., LTD. - 8010379.
- Total reports
- 6,663
- Deaths
- 13
- Injuries
- 6,504
- Malfunctions
- 143
Reports per year
210
2611
7612
3,79113
1,18114
1,58715
Source: FDA adverse event reports by year received, 2010–2015. 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)KWA4,746
- Prosthesis, Hip, Femoral, ResurfacingKXA1,633
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY148
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI57
- Prosthesis, Hip, Femoral Component, Cemented, MetalJDG46
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH19
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO6
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or UncementedMRA2
- Prosthesis, Hip, Hemi-, Trunnion-Bearing, Femoral, Metal/PolyacetalJDH1
- Prosthesis, Hip, Cement RestrictorJDK1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Depuy Intl., Ltd. - 8010379 automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.