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
- 147,658
- Deaths
- 235
- Injuries
- 90,393
- Malfunctions
- 57,028
Reports per year
2,93712
4,27013
3,37014
3,88315
2,04916
3,22617
7,39418
18,39819
16,92720
18,56221
16,55222
16,30123
14,74324
11,97625
6,03426
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH26,509
- ReamerHTO19,467
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA15,840
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH15,634
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI13,773
- ImpactorHWA6,208
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL5,691
- TemplateHWT5,313
- Orthopedic Manual Surgical InstrumentLXH5,105
- Bit, DrillHTW4,889
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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