Depuy Orthopaedics Inc US
FDA adverse event reports naming Depuy Orthopaedics Inc US as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DePuy Orthopaedics Inc US.
- Total reports
- 1,267
- Deaths
- 0
- Injuries
- 785
- Malfunctions
- 482
Top device categories
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH276
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH145
- Orthopedic Manual Surgical InstrumentLXH85
- ImpactorHWA79
- Bit, DrillHTW71
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO66
- Prosthesis, Shoulder, Hemi-, Humeral, Metallic UncementedHSD57
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI57
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL48
- Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/PolymerHSN45
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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