Class IIReported 2026-04-01
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System
Recalled by Orthalign, Inc
Reason for Recall
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
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Recall NumberZ-1629-2026ClassificationClass IIStatusOngoingCategorydeviceInitiated2026-02-10Reported2026-04-01DistributionUS Nationwide distribution in the state of UT.Code InfoLot # 25091103BB/ UDI: 00810832032427Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.