Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm. The Illico Recalled by Alphatec Spine, Inc. Due to The firm initiated this recall of certain lots...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Alphatec Spine, Inc. directly.
Affected Products
Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm. The Illico MIS Posterior Fixation System is intended to facilitate the surgical correction of noncervical spinal deformities by providing temporary internal fixation and stabilization during bone graft healing and/or fusion mass development.
Quantity: 333 screws
Why Was This Recalled?
The firm initiated this recall of certain lots of Illico Ti Cannulated Polyaxial Screws 7.5mm x 40mm implants, due to an off-center cannulation hole at the proximal end of the bone screw. There is a potential risk that when the screw is mated to a polyaxial screwdriver, the guide wire may not pass through the screwdriver.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Alphatec Spine, Inc.
Alphatec Spine, Inc. has 45 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report