Official recall notice
FDA DeviceClass IINotable
FDA Recall: Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
- Recall date
- 2026-04-01
- Brand
- Orthalign, Inc
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
Recommended action
What to do
7 units
Product description
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)