Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Anjon Bremer Molded Crown. bone fixation fastener for spinal use. Recalled by Anjon Holdings Due to High rate of galling of one threaded component.
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 Anjon Holdings directly.
Affected Products
Anjon Bremer Molded Crown. bone fixation fastener for spinal use. REF number 100048 - Product Usage: Smooth or threaded metallic bone fixation fastener. Provides cervical spine immobilization and therapeutic traction for treatment of patients with cervical trauma or other neck conditions.
Quantity: 249 devices
Why Was This Recalled?
High rate of galling of one threaded component.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Anjon Holdings
Anjon Holdings 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