PILLAR SA TiRecalls & reported problems across all models
Orthofix US LLC · 3 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one PILLAR SA Ti model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 3 models of PILLAR SA Ti by Orthofix US LLC in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
PILLAR SA Ti recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Feb 20, 2025Open, Classified
The product is mislabeled with the incorrect anterior height of 10mm, but the laser marking on the implant and corresponding trial both show the correct anterior height of 10.5mm.
Z-1432-2025 · Root cause: Labeling Change Control · names 3 of these models · Recall details · FDA record ↗
PILLAR SA Ti models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- PILLAR SA Ti 82-3300SPIntervertebral fusion device with bone graft, lumbar1 recall0 reports
- PILLAR SA Ti 82-3700SPIntervertebral fusion device with bone graft, lumbar1 recall0 reports
- PILLAR SA Ti 82-4000SPIntervertebral fusion device with bone graft, lumbar1 recall0 reports
Other Orthofix US LLC products
- CONNECTOR2 models · 0 reports · 2 recalls
- FORZA PTC76 models · 3 reports · 1 recall
- Firebird SI Fusion20 models · 1 reports · 1 recall
- CONSTRUX - MINI PTC70 models · 0 reports · 1 recall
- PILLAR SA PTC16 models · 0 reports · 1 recall
- FORZA Ti91 models · 0 reports · 1 recall
- CONSTRUX - MINI Ti112 models · 0 reports · 1 recall
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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