Drug recall
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System
FDA recall event 98516 · Class II · Orthalign, Inc
Key facts
| Event ID | 98516 |
|---|---|
| Recall numbers | Z-1629-2026, Z-1630-2026 |
| Recalling firm | Orthalign, Inc |
| Product type | Devices |
| Products | Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System, Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm) |
| Initiation date | Feb 10, 2026 |
| Report date | Apr 1, 2026 |
| City | Aliso Viejo |
| State | CA |
| Country | United States |
| FEI number | 3007521480 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: