WhichRecall
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 Number
Z-1629-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2026-02-10
Reported
2026-04-01
Distribution
US Nationwide distribution in the state of UT.
Code Info
Lot # 25091103BB/ UDI: 00810832032427
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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