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
- 42,283
- Deaths
- 88
- Injuries
- 35,139
- Malfunctions
- 7,055
Reports per year
3312
4,24413
5,05614
4,50515
4,05616
3,77417
4,16418
4,12719
2,72420
2,08121
1,94422
1,59723
1,78524
1,53425
65326
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH10,097
- Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerMBH7,087
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI6,484
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH5,374
- Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium PhosphateMEH3,434
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO1,692
- Orthopedic Manual Surgical InstrumentLXH1,566
- Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/PolymerKRO1,155
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA952
- Bone CementLOD872
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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