Recall
FDAHealthFebruary 10, 2026

Orthalign, Inc — Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System

⚠️ Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
February 10, 2026

US Nationwide distribution in the state of UT.

What's affected?

Product
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
Lot code
25092204BB/

Additional details

Lot # 25092204BB/ UDI:00810832032434

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 7 units.

View original FDA notice →

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