PROFEMURRecalls & reported problems across all models
Microport Orthopedics Inc. · 116 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
PROFEMUR models — page 2
116 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- PROFEMUR® PRGLCLE7Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- PROFEMUR® PRGLCLE8Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- PROFEMUR® PRGLCLS6Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- PROFEMUR® PRGLSTBRBROACH1 report
- PROFEMUR® PRLX5813Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- PROFEMUR® PRNEPLUGEXTRACTOR1 report
- PROFEMUR® PRPR0005Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- PROFEMUR PRTL2E03Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 report
- PROFEMUR® PRTLE025Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- PROFEMUR® PRTLE027Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- PROFEMUR® PRTLE028Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented1 report
- PROFEMUR® PRTLEL24Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented1 report
- PROFEMUR® PRTLS023Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- PROFEMUR® PRTLS025Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- PROFEMUR® PRTLS029Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- PROFEMUR® PRXMDC01Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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