Stryker Orthopaedics Mahwah
FDA adverse event reports naming Stryker Orthopaedics Mahwah as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER ORTHOPAEDICS MAHWAH.
- Total reports
- 8,203
- Deaths
- 11
- Injuries
- 4,927
- Malfunctions
- 3,197
Reports per year
4104
13805
15206
19007
39308
85509
1,87110
1,80511
2,54912
16413
4414
115
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
- Orthopedic Manual Surgical InstrumentLXH2,076
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH1,468
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI1,176
- Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium PhosphateMEH994
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH354
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO269
- Prosthesis, Knee, Hemi-, Tibial, Resurfacing (Uncemented)HSH267
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY212
- Prosthesis, Hip, Hemi-, Acetabular, Cemented, MetalKWB211
- Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/PolymerKWZ121
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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