FDA recall Z-1629-2026

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)

Distribution

US Nationwide distribution in the state of UT.

Key facts

Status

Ongoing

Initiation date

2026-02-10

Report date

2026-04-01

Voluntary/Mandated

Voluntary: Firm initiated

Location

Aliso Viejo, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1629-2026