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
- 1,134
- Deaths
- 2
- Injuries
- 1,130
- Malfunctions
- 2
Reports per year
43015
54416
16017
Source: FDA adverse event reports by year received, 2015–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA777
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI176
- Prosthesis, Hip, Femoral, ResurfacingKXA58
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY52
- Prosthesis, Hip, Femoral Component, Cemented, MetalJDG28
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH14
- Prosthesis, Hip, Hemi-, Femoral, MetalKWL7
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO7
- Prosthesis, Shoulder, Hemi-, Humeral, Metallic UncementedHSD4
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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