Innovasis recalls LS-749 pedicle screw part for potential surgical delays. The anti-torque instrument may not engage properly during tightening, requiring alternative procedures.
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.
Innovasis is recalling a specific part (LS-749) of their Vector Pedicle Screw System due to a risk that it might not engage correctly during spinal surgery, potentially causing delays or needing alternative procedures.
The LS-749 anti-torque instrument may have an undersized condition that prevents the tip from properly engaging with the pedicle screw during tightening. This could lead to surgical delays or the need for alternative methods to complete the final tightening step.
Surgical teams using Innovasis Vector Pedicle Screw System parts for spinal fusion procedures. Patients undergoing spinal surgery with this specific part are most at risk.
Check if your Vector Pedicle Screw System includes part LS-749 with UDI-DI codes M711BTA2020 or M711LS7490 and serial numbers 002, 003, 007, 012, or 014.
Identify if your Vector Pedicle Screw System includes part LS-749 with the specified UDI-DI codes and serial numbers.
Yes, the LS-749 is part of the Vector Pedicle Screw System used for spinal fusion procedures.
The part may not engage properly during tightening, potentially causing surgical delays or requiring alternative procedures.
Check for UDI-DI codes M711BTA2020 or M711LS7490 and serial numbers 002, 003, 007, 012, or 014 on the part.
We’ve drafted a message you can send Innovasis to request your refund or repair — edit it as you like.
Subject: Recall Z-2859-2026 — Innovasis Innovasis Hello, I own a Innovasis that is covered by recall Z-2859-2026 from Innovasis. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
