Depuy CMW - 9610921
FDA adverse event reports naming Depuy CMW - 9610921 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY CMW - 9610921.
- Total reports
- 2,852
- Deaths
- 11
- Injuries
- 2,456
- Malfunctions
- 385
Reports per year
110
315
416
917
9718
74619
97220
62421
14422
4423
8124
6325
6426
Source: FDA adverse event reports by year received, 2010–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Bone CementLOD2,064
- Bone Cement, AntibioticMBB742
- BroachHTQ19
- Dispenser, CementKIH10
- Prosthesis, Hip, Cement RestrictorJDK5
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH4
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL2
- Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/PolymerHRY1
- Mixer, Cement, For Clinical UseJDZ1
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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