Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Non-Sterile Double Ended Trial Kit Recalled by restor3d Inc. Due to Product labeled incorrectly. The lot was labeled with...
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 restor3d Inc. directly.
Affected Products
Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes 3 trials. Orthopedic manual surgical instrument
Quantity: 14 units
Why Was This Recalled?
Product labeled incorrectly. The lot was labeled with Small footprint when the product was Medium.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About restor3d Inc.
restor3d Inc. 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