FDA recall, , Moderate risk
Innovasis Vector Pedicle Screw System Anti-Torque
The anti-torque instrument may have an undersized condition that could prevent it from engaging with the screw, leading to surgical delay.
Summary by Recall Canary from the FDA notice
What happened
Innovasis, Inc, of Salt Lake City, Utah, recalled the Anti-Torque, Vector, Part LS-749, part of the Vector Pedicle Screw System, on May 22, 2026. The FDA added the recall to its Enforcement Report on August 3, 2026.
The pedicle screw system, intended for spinal fusion, may have an anti-torque instrument with an undersized condition that could prevent the mating tip from engaging with the pedicle screw tulip and rod during tightening, potentially causing surgical delay or intervention/alternative methods to perform final tightening step. Distribution was in the states of TX, CA.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Compare these details with yours, then check the recall notice to see which units are recalled.
Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the states of Texas, California.
- Company
- Innovasis, IncSalt Lake City, Utah
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99188
- Recall number
- Z-2859-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
