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
- 42,203
- Deaths
- 88
- Injuries
- 35,064
- Malfunctions
- 7,050
Reports per year
3412
4,24413
5,05614
4,50515
4,05616
3,77417
4,16418
4,12719
2,72520
2,08121
1,94422
1,59923
1,78524
1,53425
56926
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH10,086
- Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerMBH7,081
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI6,466
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH5,358
- Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium PhosphateMEH3,433
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO1,687
- Orthopedic Manual Surgical InstrumentLXH1,566
- Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/PolymerKRO1,140
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA952
- Bone CementLOD873
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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