FDAFebruary 10, 2026device
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
What to do
FDA enforcement status: Ongoing
Brands named
orthalign
UPCs
00810832032434
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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