Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ceres-C Standalone Cervical Interbody The product is a stand-alone anterior Recalled by Amendia, Inc Due to Absent tantalum market pin.
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 Amendia, Inc directly.
Affected Products
Ceres-C Standalone Cervical Interbody The product is a stand-alone anterior cervical interbody fusion device indicated for use in skeletally mature patients with degenerative disc disease (DDD) with accompanying radicular symptoms at the one level from C2-T1.
Quantity: 6 devices
Why Was This Recalled?
Absent tantalum market pin.
Where Was This Sold?
This product was distributed to 1 state: GA
About Amendia, Inc
Amendia, Inc has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report