FDAFDA · Food and drugs·Recall number Z-1630-2026
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
Published April 1, 2026 · Recall initiated: February 10, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Orthalign, Inc
- Distributor
- US Nationwide distribution in the state of UT.
- Lot
- Lot # 25092204BB/ UDI:00810832032434
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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