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Orthalign, Inc recalls Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
Recalled April 1, 2026 · FDA recall Z-1630-2026 · Orthalign
Hazard
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm) · FDA Class II
Units
7 units
Sold at
US Nationwide distribution in the state of UT.
Description
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
Product
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
Manufacturer(s)
Orthalign, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →