1219655 Depuy-raynham, A DIV. OF Depuy Orthopaedic
FDA adverse event reports naming 1219655 Depuy-raynham, A DIV. OF Depuy Orthopaedic as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: 1219655 DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDIC.
- Total reports
- 1,594
- Deaths
- 0
- Injuries
- 1,352
- Malfunctions
- 242
Reports per year
210
111
512
45513
24314
60415
20616
7817
Source: FDA adverse event reports by year received, 2010–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH706
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL271
- Orthopedic Manual Surgical InstrumentLXH192
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH138
- Screw, Fixation, Bone, Non-Spinal, MetallicNDJ64
- Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/PolymerHRY55
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA48
- Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/PolymerKRO34
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI24
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY11
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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