Orthalign, Inc
2
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-04-01 to 2026-04-01
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-04-01 | FDA Device | FDA Recall: Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System | Orthalign, Inc | Class II | N/A |
| 2026-04-01 | FDA Device | FDA Recall: Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System | Orthalign, Inc | Class II | N/A |