Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures Recalled by SPINEART SA Due to Inner blister pack label is incorrect and does...
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 SPINEART SA directly.
Affected Products
Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures
Quantity: 14 pieces distribtued to 1 US Distributor
Why Was This Recalled?
Inner blister pack label is incorrect and does not match the correct external box label.
Where Was This Sold?
This product was distributed to 1 state: CA
About SPINEART SA
SPINEART SA has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report