Depuy Ireland - 3015516266
FDA adverse event reports naming Depuy Ireland - 3015516266 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY IRELAND - 3015516266.
- Total reports
- 9,526
- Deaths
- 2
- Injuries
- 2,876
- Malfunctions
- 6,648
Reports per year
7821
40022
1,58323
2,47924
2,95725
2,02926
Source: FDA adverse event reports by year received, 2021–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Orthopedic Manual Surgical InstrumentLXH1,943
- TemplateHWT1,256
- ImpactorHWA1,020
- Shoulder Prosthesis, Reverse ConfigurationPHX713
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH689
- Driver, ProsthesisHWR623
- Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, UncementedMBF445
- Tray, Surgical, InstrumentFSM435
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO380
- Bone CementLOD285
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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