Depuy-raynham, A Division OF Depuy Orthopaedics, Inc.
FDA adverse event reports naming Depuy-raynham, A Division OF Depuy Orthopaedics, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC..
- Total reports
- 2,431
- Deaths
- 1
- Injuries
- 2,333
- Malfunctions
- 88
Reports per year
600
2301
10802
7803
6504
20405
16706
16107
25808
52109
49210
34811
Source: FDA adverse event reports by year received, 2000–2011. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH1,365
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL269
- Screw, Fixation, Bone, Non-Spinal, MetallicNDJ131
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH82
- Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/PolymerHRY81
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI81
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA70
- Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/PolymerKRO54
- Orthopedic Manual Surgical InstrumentLXH54
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY39
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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