Spinal FrontiersPowered by NSpineFive anti-torque instruments may be undersized and fail to engage the tulip and rod during final tightening, which could delay surgery. Initiated in May but only posted by FDA on 3 August.
- Type
- Recall
- Company
- Innovasis
- Device
- Anti-torque instrument LS-749, Vector Pedicle Screw System
- Date
- 3 August 2026
- Jurisdiction
- US
- Classification
- FDA Class II recall (Z-2859-2026)
- Source
- FDA Medical Device Recalls database
Read the official notice →Source checked
What to do
Act on the regulator's or manufacturer's own notice; this page is a summary, not an official safety channel. If a device has failed or harmed a patient, see Report a Device Problem for who to tell in your country.