Depuy International
FDA adverse event reports naming Depuy International as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY INTERNATIONAL.
- Total reports
- 30,023
- Deaths
- 52
- Injuries
- 29,859
- Malfunctions
- 97
Reports per year
199
100
305
106
207
108
309
1810
5,88711
19,15312
4,95113
115
116
Source: FDA adverse event reports by year received, 1999–2016. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA25,853
- Prosthesis, Hip, Femoral, ResurfacingKXA2,524
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI905
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH330
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY205
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO91
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or UncementedMRA26
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL24
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH19
- Prosthesis, Hip, Femoral Component, Cemented, MetalJDG9
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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