FDA Device recall Z-2859-2026
Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System
- FDA Device
- Class II
- ongoing
- Published 2026-08-12
On 2026-08-12 the FDA classified a Class II recall of Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System by Innovasis, citing 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 und….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2859-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-05-22 |
| Published | 2026-08-12 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Innovasis |
| Distribution | US |
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.
Identifiers
| code_info | LS-749: UDI-DI: M711BTA2020, M711LS7490, Serial Numbers: 002, 003, 007, 012, 014 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2859-2026%22
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