Depuy Intl., Ltd.
FDA adverse event reports naming Depuy Intl., Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY INTL., LTD..
- Total reports
- 1,148
- Deaths
- 0
- Injuries
- 1,130
- Malfunctions
- 16
Reports per year
104
5409
22810
64311
8612
13413
214
Source: FDA adverse event reports by year received, 2004–2014. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA823
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI174
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH58
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY30
- Prosthesis, Hip, Femoral, ResurfacingKXA26
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO11
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL6
- Prosthesis, Hip, Hemi-, Acetabular, Cemented, MetalKWB5
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or UncementedMRA5
- Prosthesis, Hip, Femoral Component, Cemented, MetalJDG3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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