Depuy Ireland - 9616671
FDA adverse event reports naming Depuy Ireland - 9616671 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY IRELAND - 9616671.
- Total reports
- 47,009
- Deaths
- 23
- Injuries
- 22,902
- Malfunctions
- 24,084
Reports per year
1612
2713
1614
6115
6716
47717
2,36018
4,72519
6,03520
6,62621
5,47922
6,09923
6,82124
5,40725
2,78726
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH13,003
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL7,080
- TemplateHWT6,629
- ImpactorHWA5,429
- Orthopedic Manual Surgical InstrumentLXH2,321
- Driver, ProsthesisHWR1,374
- BroachHTQ1,295
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH1,128
- ReamerHTO898
- Prosthesis, Shoulder, Hemi-, Humeral, Metallic UncementedHSD779
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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