Class II
Medical Device Recall: Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
Orthalign, Inc · February 10, 2026
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.
States Affected
NATIONWIDE
Quantity Affected
7 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1630-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.