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
- 1,314
- Deaths
- 3
- Injuries
- 1,238
- Malfunctions
- 73
Reports per year
110
2313
23414
34115
39916
30517
118
919
120
Source: FDA adverse event reports by year received, 2010–2020. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Bone CementLOD1,238
- Bone Cement, AntibioticMBB42
- Orthopedic Manual Surgical InstrumentLXH10
- Mixer, Cement, For Clinical UseJDZ6
- Catheter And Tip, SuctionJOL5
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH3
- Prosthesis, Hip, Cement RestrictorJDK2
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL2
- Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/PolymerHSX1
- Prosthesis, Elbow, Semi-Constrained, CementedJDB1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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