medical MODERATE Updated 2026-08-12

Innovasis, Inc recalls Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Scr

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Recalled Product

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

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Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: LS-749: UDI-DI: M711BTA2020, M711LS7490, Serial Numbers: 002, 003, 007, 012, 014

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
View official government recall