Anti-Torque recall
Innovasis, Inc recalled Anti-Torque on August 12, 2026 because of 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. It was sold nationwide.
Why it was recalled
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's recalled
Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System
Quantity: 5
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Innovasis, Inc, Salt Lake City, UT
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
US Nationwide distribution in the states of TX, CA. - Status
- Ongoing
- Recall number
- Z-2859-2026
- Source
- U.S. Food and Drug Administration
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