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
- 10,629
- Deaths
- 13
- Injuries
- 10,366
- Malfunctions
- 231
Reports per year
600
2101
3002
4303
5004
15105
19606
27207
45708
71109
1,94510
6,74111
512
113
Source: FDA adverse event reports by year received, 2000–2013. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA7,958
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI1,297
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH258
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY233
- Prosthesis, Hip, Femoral, ResurfacingKXA219
- Prosthesis, Hip, Hemi-, Acetabular, Cemented, MetalKWB156
- Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/PolymerHRY126
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO87
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL51
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or UncementedMRA42
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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