Stryker Orthopaedics Cork
FDA adverse event reports naming Stryker Orthopaedics Cork as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER ORTHOPAEDICS CORK.
- Total reports
- 5,035
- Deaths
- 3
- Injuries
- 3,964
- Malfunctions
- 1,024
Reports per year
4704
12105
12806
16607
41408
63109
84210
83311
1,35312
15813
33214
1015
Source: FDA adverse event reports by year received, 2004–2015. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium PhosphateMEH2,274
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI607
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO581
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or UncementedMRA371
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY246
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH210
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH208
- Prosthesis, Knee, Hemi-, Tibial, Resurfacing (Uncemented)HSH144
- Orthopedic Manual Surgical InstrumentLXH105
- Prosthesis, Hip, Hemi-, Acetabular, Cemented, MetalKWB61
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Stryker Orthopaedics Cork automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.