Innovasis, Inc recalls Anti-Torque
- Recalling company
- Innovasis, Inc
- Product
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- May 22, 2026
- Reported
- Aug 12, 2026
- Distribution
- US Nationwide distribution in the states of TX, CA.
- Status
- Ongoing
- Quantity
- 5
- Lot / codes
- LS-749: UDI-DI: M711BTA2020, M711LS7490, Serial Numbers: 002, 003, 007, 012, 014
- Company location
- Salt Lake City, UT
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2859-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2859-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.