FDA DeviceClass IINotable

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

Date: 2026-04-01
Brand: Orthalign, Inc
Category: Medical Device
FDA Class: Class II

Description

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

Hazard

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

Remedy

7 units

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