Orthalign Drill Plate Lantern Knee System Recall
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System
Updated February 10, 2026
Orthalign's Drill Plate component for the Lantern Knee System can be manufactured out of specification, causing bone cuts larger than intended during surgery. This could affect surgical accuracy and patient outcomes.
Is the Orthalign, Inc recalled? Yes. This product was recalled by FDA on February 10, 2026. Details below.
What is recalled
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1-5, Reference Number 402566, which is a component of the Lantern Knee System.
Am I affected
You are affected if your healthcare facility or surgical center has this drill plate component in inventory. Check for Reference Number 402566 on the packaging or product documentation.
What to do right now
If you are a healthcare provider or facility using this device, stop using affected units and contact Orthalign, Inc. directly to identify which products are affected and arrange for replacement or inspection.
The hazard
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
Brands affected
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-1629-2026
- Classification
- Class II
- Recalled
- February 10, 2026
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