8010379 Depuy Intl., Ltd.
FDA adverse event reports naming 8010379 Depuy Intl., Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: 8010379 DEPUY INTL., LTD..
- Total reports
- 1,406
- Deaths
- 2
- Injuries
- 1,404
- Malfunctions
- 0
Reports per year
110
411
512
90613
11714
24215
12616
517
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, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA690
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI508
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH121
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO27
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY23
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH6
- Prosthesis, Hip, Femoral, ResurfacingKXA6
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL5
- Prosthesis, Hip, Femoral Component, Cemented, MetalJDG4
- Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/PolymerHRY3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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