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Medium risk Drugs & MedicationsClass II

Orthalign, Inc Recall

Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System

Updated February 10, 2026

Orthalign, Inc is recalling Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System. Hazard: Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)

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 REF:402566 component Lantern Knee System

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

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
Drugs & Medications
Recall ID
fda-Z-1629-2026
Classification
Class II
Recalled
February 10, 2026
Read the official notice

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