Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft Recalled by Spine Smith Partners LP Due to Implants were incorrectly laser marked as 23mm instead...
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 Spine Smith Partners LP directly.
Affected Products
Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemental fixation.
Quantity: 3 units
Why Was This Recalled?
Implants were incorrectly laser marked as 23mm instead of 28mm.
Where Was This Sold?
Distributed in Texas.
About Spine Smith Partners LP
Spine Smith Partners LP has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report