Sulzer Orthopedics, Inc.
FDA adverse event reports naming Sulzer Orthopedics, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SULZER ORTHOPEDICS, INC..
- Total reports
- 1,861
- Deaths
- 1
- Injuries
- 1,801
- Malfunctions
- 11
Reports per year
3197
2998
2499
5700
1,40601
31002
403
Source: FDA adverse event reports by year received, 1997–2003. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH815
- Prosthesis, Knee, Hemi-, Tibial, Resurfacing (Uncemented)HSH789
- Prosthesis, Hip, Hemi-, Acetabular, Cemented, MetalKWB79
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH56
- Prosthesis, Knee, Hemi-, Patellar Resurfacing, UncementedHTG22
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI22
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY18
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA17
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO11
- Prosthesis, Knee, Hemi-, FemoralHSA5
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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