Reported Apr 1, 2026 · Ongoing
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System
Orthalign, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Orthalign, Inc · 120 Columbia Ste 500 · Aliso Viejo, CA · 92656-4107
Is this the product you have?
- Drill Plate, Ortho Dev. Trimax - Pegged
- PREF Size 1 -5 REF402566 component Lantern Knee System
- Lot codes and dates
- Lot # 25091103BB/
- UDI00810832032427
- Amount recalled
- 7 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
- UT
Why it was recalled
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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