← Back to Medical Device Recalls
Recall Category: Medical Device Recalls
Recalling Firm: Orthalign, Inc
Product: Drill Plate, Ortho Dev. Trimax – Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System
Reason for Recall: Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
Classification: Class II
Status: Ongoing
Report Date: 04/01/2026
Recall Initiation Date: 02/10/2026
Distribution: US Nationwide distribution in the state of UT.
Code Info: Lot # 25091103BB/ UDI: 00810832032427
Product Quantity: 7 units
Recall Type: Voluntary: Firm initiated
Initial Firm Notification: Letter
Firm Location: Aliso Viejo, CA, United States
Recall Number: Z-1629-2026
Event ID: 98516