Skip to main content
Recall Canary
Vector Pedicle Screw System Anti-Torque
← Back to all recalls
MEDICAL DEVICE RECALLMODERATE

Vector Pedicle Screw System Anti-Torque

Innovasis recalls Vector Pedicle Screw System anti-torque instrument (LS-749) due to undersized tip that may prevent engagement during surgery.

What to do

If you have this anti-torque instrument, stop using it and contact Innovasis for instructions on returning the affected device and obtaining a replacement.

Recalled
Listed
Updated
Recall No.
Z-2859-2026
Agency
FDA
Firm
Innovasis, Inc
Recall ID
99188
Status
ONGOING

Why it was recalled

Innovasis is recalling the Anti-Torque instrument (Part LS-749) used with the Vector Pedicle Screw System. The anti-torque instrument may be undersized, preventing the mating tip from engaging with the pedicle screw tulip and rod during tightening, which could lead to surgical delay and require alternative methods to complete the final tightening step.

Is mine affected?

This recall covers the product below. If you have it, yours is affected.

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

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Other Device Defect recalls

← Back to all recalls

Editorial summary by Recall Canary · summary updated 2026-08-04 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification