Orthalign Drill Plate Recall 402567
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
Updated February 10, 2026
Orthalign's Drill Plate component for the Lantern Knee System (Trimax, Size 6-7, REF 402567) may be manufactured out of specification, causing the device to cut bone deeper than intended during surgery.
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 6-7, REF 402567, a component of the Lantern Knee System manufactured by Orthalign, Inc.
Am I affected
You are affected if you have a Lantern Knee System that uses the Trimax Drill Plate component with reference number 402567 in size 6-7 PREF.
What to do right now
Contact Orthalign, Inc immediately if you have received or used this drill plate component. Do not use the device until you have confirmed with the manufacturer whether your unit is affected.
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-1630-2026
- Classification
- Class II
- Recalled
- February 10, 2026
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