Depuy Warsaw
FDA adverse event reports naming Depuy Warsaw as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY WARSAW.
- Total reports
- 7,541
- Deaths
- 6
- Injuries
- 7,369
- Malfunctions
- 164
Reports per year
109
210
2,13211
5,25712
14913
Source: FDA adverse event reports by year received, 2009–2013. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH2,082
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH1,417
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA974
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI957
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY470
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL413
- Orthopedic Manual Surgical InstrumentLXH138
- Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer CementedKWS91
- Screw, Fixation, BoneHWC75
- Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)JDL69
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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