Depuy International Ltd.
FDA adverse event reports naming Depuy International Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY INTERNATIONAL LTD..
- Total reports
- 1,663
- Deaths
- 7
- Injuries
- 1,626
- Malfunctions
- 30
Reports per year
100
104
1205
806
1207
1208
6609
2310
10211
11212
64013
42014
13615
3816
8017
Source: FDA adverse event reports by year received, 2000–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA1,113
- Prosthesis, Hip, Femoral, ResurfacingKXA344
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI107
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY32
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH27
- Prosthesis, Hip, Hemi-, Acetabular, Cemented, MetalKWB10
- Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/PolymerHRY7
- Prosthesis, Hip, Femoral Component, Cemented, MetalJDG6
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO6
- 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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