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
- 46,715
- Deaths
- 23
- Injuries
- 22,769
- Malfunctions
- 23,923
Reports per year
1612
2713
1614
6115
6716
47717
2,36118
4,72519
6,03520
6,62621
5,47922
6,09923
6,82124
5,40725
2,49226
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH12,908
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL7,057
- TemplateHWT6,596
- ImpactorHWA5,401
- Orthopedic Manual Surgical InstrumentLXH2,290
- Driver, ProsthesisHWR1,367
- BroachHTQ1,292
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH1,122
- ReamerHTO898
- Prosthesis, Shoulder, Hemi-, Humeral, Metallic UncementedHSD776
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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