Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System
| Source | FDA Device Enforcement |
|---|---|
| Category | Medical Device |
| Severity | Medium |
| Status | ongoing |
| Recall date | February 10, 2026 |
| Reported | April 01, 2026 |
| Recalling firm | Orthalign, Inc |
| Country / region | United States CA |
Hazard
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
Affected products
- Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System
Related recalls
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