Depuy Orthopaedics Inc US 1818910
FDA adverse event reports naming Depuy Orthopaedics Inc US 1818910 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY ORTHOPAEDICS INC US 1818910.
- Total reports
- 1,300
- Deaths
- 0
- Injuries
- 727
- Malfunctions
- 573
Reports per year
211
313
1317
1,28218
Source: FDA adverse event reports by year received, 2011–2018. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- ReamerHTO169
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH152
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH143
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI117
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA115
- Orthopedic Manual Surgical InstrumentLXH109
- BroachHTQ55
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or UncementedMRA46
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO43
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL37
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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