CONSTRUX - MINI TiRecalls & reported problems across all models
Orthofix US LLC · 112 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
CONSTRUX - MINI Ti models — page 2
112 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- CONSTRUX - MINI Ti 37-8308SPIntervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-8309SPIntervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-8310SPIntervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-8311SPIntervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-8312SPIntervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-9306SPIntervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-9307SPIntervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-9308SPIntervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-9309SPIntervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-9310SPIntervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-9311SPIntervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-9312SPIntervertebral fusion device with bone graft, cervical1 recall0 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page