Zimmer Orthopaedic MFG. Ltd.
FDA adverse event reports naming Zimmer Orthopaedic MFG. Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ZIMMER ORTHOPAEDIC MFG. LTD..
- Total reports
- 3,408
- Deaths
- 1
- Injuries
- 2,766
- Malfunctions
- 641
Reports per year
5116
11817
21318
34419
32420
31321
33122
35123
54324
54425
27626
Source: FDA adverse event reports by year received, 2016–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH1,747
- Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerMBH1,517
- Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/PolymerHSX58
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile BearingNJL57
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + AdditiveOIY17
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH5
- Rod, Fixation, Intramedullary And AccessoriesHSB2
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI2
- Prosthesis, Shoulder, Hemi-, Humeral, Metallic UncementedHSD1
- Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/PolymerKRO1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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