Innovasis Anti-Torque Instrument Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Innovasis, Inc. is recalling five units of the Anti-Torque, Vector (Part LS-749) due to a potential undersized condition that may prevent proper engagement during spinal surgery.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 19, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Innovasis, Inc. initiated a voluntary recall of the Anti-Torque, Vector instrument because it may have an undersized condition that could prevent the mating tip from engaging with the pedicle screw tulip and rod during tightening. This issue may lead to surgical delay or require alternative methods to perform the final tightening step.
Which Products Are Affected
The recall affects the Anti-Torque, Vector, Part: LS-749, which is part of the Vector Pedicle Screw System. Five units are involved, with serial numbers 002, 003, 007, 012, and 014. The UDI-DIs are M711BTA2020 and M711LS7490. Distribution was limited to US Nationwide in the states of TX and CA.
What You Should Do
Consumers and healthcare providers should follow instructions provided in the firm's notification letter for returns or further guidance. Contact Innovasis, Inc. at 614 E 3900 S, Salt Lake City, UT 84107-1902 for additional information.
Why This Matters
The recall addresses a manufacturing condition that could affect the use of the pedicle screw system during spinal fusion procedures.
Source
FDA recall number Z-2859-2026. Classification: Class II. Event ID: 99188.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,182 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 19, 2026.
Frequently Asked Questions
Common questions about this FDA recall.