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
- 14,442
- Deaths
- 123
- Injuries
- 13,924
- Malfunctions
- 390
Reports per year
208
309
6310
76911
1,17912
1,09413
3,83714
1,98615
1,88616
1,59617
1,03418
99019
320
Source: FDA adverse event reports by year received, 2008–2020. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA8,775
- Prosthesis, Hip, Femoral, ResurfacingKXA2,757
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI1,416
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY540
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH223
- Prosthesis, Hip, Femoral Component, Cemented, MetalJDG165
- Driver, ProsthesisHWR96
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO84
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL71
- ImpactorHWA55
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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