Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SpineNet Anterior Cervical Cage Recalled by SpineNet Due to The recall decision has been made because because...
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 SpineNet directly.
Affected Products
SpineNet Anterior Cervical Cage, Lordotic, Peek (originally submitted as Daytona Anterior Cervical Cage) Product Usage: Is indicated for use in skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level
Quantity: 400
Why Was This Recalled?
The recall decision has been made because because it has recently been determined that the instructions for use (IFU) had certain statements that should have been removed prior to initial product marketing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About SpineNet
SpineNet has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report