Orthalign, Inc
Device Recalls (Class II)
Class II
Z-1630-2026
·
20260401
·
Ongoing
Product
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
Reason for Recall
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
Distribution
US Nationwide distribution in the state of UT.
Source: openFDA Enforcement API