Depuy Orthopaedics, Inc. 1818910
FDA adverse event reports naming Depuy Orthopaedics, Inc. 1818910 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY ORTHOPAEDICS, INC. 1818910.
- Total reports
- 35,260
- Deaths
- 33
- Injuries
- 24,592
- Malfunctions
- 10,629
Reports per year
3709
4710
60811
1,39712
2,04013
2,70114
2,89615
3,22116
5,67517
6,86218
9,42419
17520
9421
3122
823
Source: FDA adverse event reports by year received, 2009–2023. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA5,988
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH4,751
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI4,658
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH4,123
- Orthopedic Manual Surgical InstrumentLXH3,863
- Bone CementLOD1,329
- ReamerHTO1,176
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL1,095
- ImpactorHWA970
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY965
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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