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
- 9,304
- Deaths
- 2
- Injuries
- 2,798
- Malfunctions
- 6,504
Reports per year
7821
40022
1,58323
2,47924
2,95725
1,80726
Source: FDA adverse event reports by year received, 2021–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Orthopedic Manual Surgical InstrumentLXH1,917
- TemplateHWT1,229
- ImpactorHWA986
- Shoulder Prosthesis, Reverse ConfigurationPHX703
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH666
- Driver, ProsthesisHWR608
- Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, UncementedMBF436
- Tray, Surgical, InstrumentFSM430
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO362
- Bone CementLOD281
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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