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
- 35,256
- Deaths
- 32
- Injuries
- 24,589
- Malfunctions
- 10,629
Reports per year
3709
4710
60511
1,39612
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 during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA5,978
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH4,753
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI4,661
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH4,123
- Orthopedic Manual Surgical InstrumentLXH3,864
- 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.
Monitor Depuy Orthopaedics, Inc. 1818910 automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.