Depuy Raynham
FDA adverse event reports naming Depuy Raynham as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY RAYNHAM.
- Total reports
- 1,691
- Deaths
- 1
- Injuries
- 1,422
- Malfunctions
- 267
Reports per year
405
108
1609
1410
39611
1,23512
2513
Source: FDA adverse event reports by year received, 2005–2013. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH543
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL222
- Orthopedic Manual Surgical InstrumentLXH197
- Screw, Fixation, Bone, Non-Spinal, MetallicNDJ99
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH94
- Thoracolumbosacral Pedicle Screw SystemNKB59
- Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)JDL52
- Appliance, Fixation, Spinal InterlaminalKWP49
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA47
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI46
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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