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Medical Device

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

Recall date: 2026-04-01 · Source: FDA_DEVICE
Brand / Firm
Orthalign, Inc
Product
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System
Reason for recall
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
Units affected
7 units
Description
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System
View official recall notice →