Optetrak LogicRecalls & reported problems across all models
Exactech, Inc. · 408 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Optetrak Logic models — page 5
408 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Optetrak Logic 02-010-06-0250Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- Optetrak Logic 02-012-65-9313Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- Optetrak Logic 02-012-60-1425Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- Optetrak Logic 02-012-60-1440Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- Optetrak Logic 02-012-60-1480Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- Optetrak Logic 02-012-60-1680Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- Optetrak Logic 02-011-06-0750TEMPLATE1 report
- Optetrak Logic 02-012-66-2000Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 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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