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
- 1,525
- Deaths
- 1
- Injuries
- 1,515
- Malfunctions
- 9
Reports per year
612
713
97014
54215
Source: FDA adverse event reports by year received, 2012–2015. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA1,277
- Prosthesis, Hip, Femoral, ResurfacingKXA172
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI30
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY28
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH15
- Prosthesis, Hip, Femoral Component, Cemented, MetalJDG3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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