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
- 2,769
- Deaths
- 3
- Injuries
- 2,117
- Malfunctions
- 648
Reports per year
311
2013
1,32514
36215
2616
1,03317
Source: FDA adverse event reports by year received, 2011–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH551
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH472
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA396
- Orthopedic Manual Surgical InstrumentLXH258
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI165
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY127
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL114
- ImpactorHWA110
- Bit, DrillHTW51
- Prosthesis, Shoulder, Hemi-, Humeral, Metallic UncementedHSD40
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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