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
- 1,432
- Deaths
- 1
- Injuries
- 1,429
- Malfunctions
- 2
Reports per year
4011
5512
8413
5314
29315
66516
24117
119
Source: FDA adverse event reports by year received, 2011–2019. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA973
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI228
- Prosthesis, Hip, Femoral, ResurfacingKXA112
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY42
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH29
- Prosthesis, Hip, Femoral Component, Cemented, MetalJDG24
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO7
- Prosthesis, Hip, Hemi-, Femoral, MetalKWL6
- Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/PolymerKWZ4
- Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/PolymerHRY1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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