Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RIGHT CORONAL BENDER Recalled by Aesculap Implant Systems LLC Due to Customized coronal rod benders may deform the implant...
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 Aesculap Implant Systems LLC directly.
Affected Products
RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.
Quantity: 2 pieces
Why Was This Recalled?
Customized coronal rod benders may deform the implant when used with the spinal system devices.
Where Was This Sold?
This product was distributed to 1 state: CO
About Aesculap Implant Systems LLC
Aesculap Implant Systems LLC has 61 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report