Biomet Orthopedics
FDA adverse event reports naming Biomet Orthopedics as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BIOMET ORTHOPEDICS.
- Total reports
- 34,434
- Deaths
- 191
- Injuries
- 32,592
- Malfunctions
- 1,619
Reports per year
707
508
21009
58610
97811
2,41512
6,02313
8,87514
4,77715
4,61216
5,90117
1118
123
224
225
Source: FDA adverse event reports by year received, 2007–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)KWA12,523
- Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerJWH5,522
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, CementedJDI3,789
- Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedLPH3,038
- Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer CementedKWS992
- Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, UncementedLZO941
- Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile BearingNRA516
- Orthopedic Manual Surgical InstrumentLXH500
- Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedKWY460
- Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerMBH447
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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