Orthalign, Inc recalls Drill Plate
- Recalling company
- Orthalign, Inc
- Product
- Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System
- Reason
- Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Feb 10, 2026
- Reported
- Apr 1, 2026
- Distribution
- US Nationwide distribution in the state of UT.
- Status
- Ongoing
- Quantity
- 7 units
- Lot / codes
- Lot # 25091103BB/ UDI: 00810832032427
- Company location
- Aliso Viejo, CA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1629-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1629-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.