Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PRECICE PLATE - Product Usage: intended for limb lengthening Recalled by Nuvasive Specialized Orthopedics Inc Due to Due to complaints of adverse events potentially related...
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
PRECICE PLATE - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
Quantity: 40 units
Why Was This Recalled?
Due to complaints of adverse events potentially related to biological safety. The complaints included report of pain and bony abnormalities at the interface between the telescoping nail segments.
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