Depuy-cork, A Division OF Depuy Orthopaedics
FDA adverse event reports naming Depuy-cork, A Division OF Depuy Orthopaedics as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS.
- Total reports
- 2,143
- Deaths
- 1
- Injuries
- 2,104
- Malfunctions
- 35
Reports per year
503
1204
13305
12206
14707
27008
46409
54310
44711
Source: FDA adverse event reports by year received, 2003–2011. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL818
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH569
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI149
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH135
- Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/PolymerHRY100
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or UncementedMRA82
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA81
- Prosthesis, Knee, Hemi-, Tibial, Resurfacing (Uncemented)HSH56
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO40
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY29
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Depuy-cork, A Division OF Depuy Orthopaedics automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.