Depuy Orthopaedic Inc, 1818910
FDA adverse event reports naming Depuy Orthopaedic Inc, 1818910 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY ORTHOPAEDIC INC, 1818910.
- Total reports
- 1,785
- Deaths
- 5
- Injuries
- 1,280
- Malfunctions
- 500
Reports per year
709
810
6011
15212
12813
6414
6915
4616
11217
1,13718
219
Source: FDA adverse event reports by year received, 2009–2019. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA365
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI318
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH281
- ReamerHTO130
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH86
- Orthopedic Manual Surgical InstrumentLXH72
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO56
- Bone CementLOD55
- Bit, DrillHTW47
- ImpactorHWA47
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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