Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
NUVASIVE MAGEC 2 Rod X.X mm XX mm Recalled by NuVasive Inc Due to Post-implantation separation of an actuator end cap 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 NuVasive Inc directly.
Affected Products
NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product Usage: comprised of a sterile single-use spinal rod that is surgically implanted using appropriate NuVasive Reline, Reline Small Stature, and Armada fixation components (i.e. Pedicle screws, hooks and/or connectors, provided non-sterile, to be sterilized by the end user).
Quantity: 3502 rods
Why Was This Recalled?
Post-implantation separation of an actuator end cap component that may expose internal components of the actuator, which could lead to hastened degeneration of the internal components and egress of Titanium alloy wear debris and resultant localized tissue discoloration.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About NuVasive Inc
NuVasive Inc has 36 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report