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FDA
Food and Drug Administration · Recall Z-2859-2026 · May 22, 2026

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

Innovasis, Inc

The hazard

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. FDA Class II recall.

The remedy

Follow FDA guidance

About this recall

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

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

Model LS-749: UDI-DI: M711BTA2020Model M711LS7490Model Serial Numbers: 002Model 003Model 007Model 012Model 014

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.