Recall Ledger

Anti-Torque recall (Innovasis, Inc)

Medical deviceClass IIOngoing

Summary: Innovasis, Inc is recalling Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System. Reason: 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.

What is being recalled

Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System

Why

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.

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US Nationwide distribution in the states of TX, CA. (states named: California, Texas)

How to tell if yours is affected

LS-749: UDI-DI: M711BTA2020, M711LS7490, Serial Numbers: 002, 003, 007, 012, 014

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-2859-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedMay 22, 2026
ReportedAugust 12, 2026
CompanyInnovasis, Inc
Company locationSalt Lake City, UT, United States
Initiated byVoluntary: Firm initiated
Quantity5

More recalls from Innovasis, Inc · all medical device recalls · recalls from May 2026

Official FDA record