Orthalign, Inc recalls Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
- Recall date
- February 10, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1630-2026
- FDA classification
- Class II
- Brand / firm
- Orthalign, Inc
- Sold / distributed
- US Nationwide distribution in the state of UT.
Why it was recalled
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
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