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
- 9,055
- Deaths
- 4
- Injuries
- 6,482
- Malfunctions
- 2,569
Reports per year
210
611
1412
5913
84414
1,32015
1,35716
1,26117
1,59718
2,18019
15320
13221
9622
3423
Source: FDA adverse event reports by year received, 2010–2023. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH2,862
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL2,286
- ImpactorHWA747
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO654
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI399
- Orthopedic Manual Surgical InstrumentLXH332
- TemplateHWT321
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH224
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA192
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or UncementedMRA180
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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