Medical Device Recall: Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System
Innovasis, Inc · May 22, 2026
Reason for Recall
Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque instrument with undersized condition which could prevent mating tip from engaging with the pedicle screw tulip and rod during tightening, which may lead to surgical delay, intervention/alternative methods to perform final tightening step.
Distribution
US Nationwide distribution in the states of TX, CA.
States Affected
NATIONWIDE
Quantity Affected
5
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2859-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.