Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Titan Spine Endoskeleton Locking Bone Screw Assembly Recalled by TITAN SPINE, LLC Due to Titan Spine is recalling specific Endoskeleton TCS Integrated...
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 TITAN SPINE, LLC directly.
Affected Products
Titan Spine Endoskeleton Locking Bone Screw Assembly, which is part of the Endoskeleton TCS Interbody Fusion Device, spinal implant. Part Numbers / Product Description: 5302-3514 / 03.5 x 14mm Locking Screws; 5302-3516 / 03.5 x 16mm Locking Screws; 502-3518 / 03.5 x 18mm Locking Screws; 5302-3814 / 03.8 x 14mm Locking Screws; 5302-3816 / 03.8 x 16 mm Locking Screws; 5302-3818 / 03.8 x 18mm Locking Screws.
Quantity: 137 units
Why Was This Recalled?
Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assembly due to the locking bone screw collars not 'locking'.
Where Was This Sold?
This product was distributed to 8 states: CA, GA, IN, MA, NY, OK, OR, TX
About TITAN SPINE, LLC
TITAN SPINE, LLC has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report