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Medium risk Medical DevicesClass II

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

Orthalign, Inc
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-1630-2026
Classification
Class II
Recalled
February 10, 2026
Read the official notice

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