Fresh Recalls

FDAClass II · Medical device · Recall Z-2859-2026 · Recalled August 12, 2026

Anti-Torque recall — Innovasis, Inc

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Anti-Torque
Company / brand
Innovasis
Lot / serial / date codes
LS-749: UDI-DI: M711BTA2020, M711LS7490, Serial Numbers: 002, 003, 007, 012, 014
Distribution
US Nationwide distribution in the states of TX, CA.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Anti-Torque

3. Open the official notice or contact

Official recall ID
Z-2859-2026
Brand
Innovasis
Classification
Class II
Units affected
5
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Salt Lake City, UT, United States
Firm address
614 E 3900 S, 84107-1902

Identifying details (verbatim from the notice)

Product codes / lots
LS-749: UDI-DI: M711BTA2020, M711LS7490, Serial Numbers: 002, 003, 007, 012, 014
Distribution
US Nationwide distribution in the states of TX, CA.
Firm notified the public via
Letter
FDA event ID
99188
Recall initiated
May 22, 2026
FDA classified
August 3, 2026
FDA report date
August 12, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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