1818910 Depuy Orthopaedics, Inc.
FDA adverse event reports naming 1818910 Depuy Orthopaedics, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: 1818910 DEPUY ORTHOPAEDICS, INC..
- Total reports
- 5,947
- Deaths
- 1
- Injuries
- 5,594
- Malfunctions
- 352
Reports per year
110
411
712
4,28213
1,07814
7515
47716
2317
Source: FDA adverse event reports by year received, 2010–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH1,369
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH1,106
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA1,016
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI562
- Orthopedic Manual Surgical InstrumentLXH388
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY344
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL270
- Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/PolymerHRY148
- Prosthesis, Hip, Femoral, ResurfacingKXA113
- Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer CementedKWS87
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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