9616671 Depuy (ireland)
FDA adverse event reports naming 9616671 Depuy (ireland) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: 9616671 DEPUY (IRELAND).
- Total reports
- 1,348
- Deaths
- 1
- Injuries
- 1,344
- Malfunctions
- 3
Reports per year
210
99213
17214
4615
12816
817
Source: FDA adverse event reports by year received, 2010–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL435
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH358
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO197
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI121
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH104
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA39
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or UncementedMRA35
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY22
- Prosthesis, Hip, Femoral, ResurfacingKXA12
- Prosthesis, Hip, Femoral Component, Cemented, MetalJDG8
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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