Official recall record
Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-05-22
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Brand on record
- Innovasis, Inc
What the authority reported
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 to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-09-16.
Record last checked against the registry on 2026-09-16.
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