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
- 1,923
- Deaths
- 6
- Injuries
- 1,854
- Malfunctions
- 60
Reports per year
411
712
1,10113
78514
2615
Source: FDA adverse event reports by year received, 2011–2015. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA1,687
- Prosthesis, Hip, Femoral, ResurfacingKXA183
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI23
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH16
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY11
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO2
- Prosthesis, Hip, Hemi-, Femoral, MetalKWL1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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