Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard Endoskeleton Recalled by TITAN SPINE, LLC Due to Titan Spine LLC, is conducting a recall on...
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 TA Implant products. 2107-0118 18mm Standard Endoskeleton Implant VBR 2107-0120 20mm Standard Endoskeleton Implant VBR 2107-0218 18mm Large Endoskeleton Implant VBR 2107-0220 20mm Large Endoskeleton Implant VBR Endoskeleton TA VBR is intended for use in the thoracolumbar spine (T1-L5) to replace all or part of a collapsed, damaged, or unstable vertebral body due to tumor or trauma.
Quantity: 92 pcs.
Why Was This Recalled?
Titan Spine LLC, is conducting a recall on the Endoskeleton TA VBR products. The labeling accompanying this device contains incorrect indications for use.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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