Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
NUVASIVE SPECIALIZED ORTHOPEDICS Recalled by Nuvasive Specialized Orthopedics Inc Due to During explantation, standard removal tools can generate sufficient...
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 Nuvasive Specialized Orthopedics Inc directly.
Affected Products
NUVASIVE SPECIALIZED ORTHOPEDICS, INC. Precice Bone Transport Antegrade Femur Trochanter 10 Degree Bend Component of the orthopedic Precice Bone Transport System of intramedullary nail, locking screws, reusable instruments, and hand-held External Remote Controller (ERC).
Quantity: 41 total units
Why Was This Recalled?
During explantation, standard removal tools can generate sufficient forces to cause distal plug to disassociate from the bone transport system.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Nuvasive Specialized Orthopedics Inc
Nuvasive Specialized Orthopedics Inc has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report