Zimmer Switzerland Manufacturing Gmbh
FDA adverse event reports naming Zimmer Switzerland Manufacturing Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ZIMMER SWITZERLAND MANUFACTURING GMBH.
- Total reports
- 2,131
- Deaths
- 8
- Injuries
- 1,854
- Malfunctions
- 269
Reports per year
111
114
216
217
118
3819
38320
66121
53922
50323
Source: FDA adverse event reports by year received, 2011–2023. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Rod, Fixation, Intramedullary And AccessoriesHSB620
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO428
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA424
- Plate, Fixation, BoneHRS159
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI91
- Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer CementedKWS57
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH50
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY36
- Screw, Fixation, BoneHWC33
- Shoulder Prosthesis, Reverse ConfigurationPHX33
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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