Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Telluride Percutaneous Rod Inserter Long Recalled by Biomet Spine, LLC Due to The Telluride Percutaneous Rod Inserter Long does not...
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 Biomet Spine, LLC directly.
Affected Products
Telluride Percutaneous Rod Inserter Long, Model #7706-1904. The Inserter is a reusable device provided within an aluminum sterilization case along with other orthopedic manual surgical instruments. The case consists of three trays of instruments, and the middle tray contains a quantity of two Inserters. The Inserter is for use as part of a Telluride System pedicle screw procedure.
Quantity: 10
Why Was This Recalled?
The Telluride Percutaneous Rod Inserter Long does not contain a feature that locks the Rod in place during use. There is a potential for the Rod to disengage from the Inserter during insertion, and could lead to harm to the patient.
Where Was This Sold?
This product was distributed to 4 states: NE, NY, OH, TX
About Biomet Spine, LLC
Biomet Spine, LLC 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